Canonical Allele Identifier: CA2262102697
Gene: MAPT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46014216_46014218delinsTTC , CM000679.2:g.46014216_46014218delinsTTC GRCh38
NC_000017.10:g.44091582_44091584delinsTTC , CM000679.1:g.44091582_44091584delinsTTC GRCh37
NC_000017.9:g.41447419_41447421delinsTTC NCBI36
NG_007398.1:g.124796_124798delinsTTC
NG_007398.2:g.124754_124756delinsTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000420682.7:c.829-27_829-25delinsTTC ENSP00000413056.2:n.829-27_829-25delinsTTC
ENST00000703922.1:c.829-27_829-25delinsTTC ENSP00000515557.1:n.829-27_829-25delinsTTC
ENST00000703923.1:c.742-27_742-25delinsTTC ENSP00000515558.1:n.742-27_742-25delinsTTC
ENST00000703924.1:c.829-27_829-25delinsTTC ENSP00000515559.1:n.829-27_829-25delinsTTC
ENST00000703978.1:c.916-27_916-25delinsTTC ENSP00000515600.1:n.916-27_916-25delinsTTC
ENST00000703979.1:n.687-27_687-25delinsTTC
ENST00000703980.1:n.142-27_142-25delinsTTC
ENST00000703981.1:n.85-27_85-25delinsTTC
ENST00000262410.10:c.2092-27_2092-25delinsTTC MANE Select ENSP00000262410.6:n.2092-27_2092-25delinsTTC
ENST00000344290.10:c.1801-27_1801-25delinsTTC ENSP00000340820.6:n.1801-27_1801-25delinsTTC
ENST00000351559.10:c.916-27_916-25delinsTTC ENSP00000303214.7:n.916-27_916-25delinsTTC
ENST00000535772.6:c.736-27_736-25delinsTTC ENSP00000443028.2:n.736-27_736-25delinsTTC
ENST00000680542.1:c.829-27_829-25delinsTTC ENSP00000505258.1:n.829-27_829-25delinsTTC
ENST00000680674.1:c.742-27_742-25delinsTTC ENSP00000505478.1:n.742-27_742-25delinsTTC
ENST00000262410.9:c.1867-27_1867-25delinsTTC ENSP00000262410.5:n.1867-27_1867-25delinsTTC
ENST00000334239.12:c.649-27_649-25delinsTTC ENSP00000334886.8:n.649-27_649-25delinsTTC
ENST00000340799.9:c.829-27_829-25delinsTTC ENSP00000340438.5:n.829-27_829-25delinsTTC
ENST00000344290.9:c.1921-27_1921-25delinsTTC ENSP00000340820.5:n.1921-27_1921-25delinsTTC
ENST00000351559.9:c.916-27_916-25delinsTTC ENSP00000303214.7:n.916-27_916-25delinsTTC
ENST00000415613.6:c.1921-27_1921-25delinsTTC ENSP00000410838.2:n.1921-27_1921-25delinsTTC
ENST00000420682.6:c.829-27_829-25delinsTTC ENSP00000413056.2:n.829-27_829-25delinsTTC
ENST00000431008.7:c.823-27_823-25delinsTTC ENSP00000389250.3:n.823-27_823-25delinsTTC
ENST00000446361.7:c.742-27_742-25delinsTTC ENSP00000408975.3:n.742-27_742-25delinsTTC
ENST00000535772.5:c.823-27_823-25delinsTTC ENSP00000443028.1:n.823-27_823-25delinsTTC
ENST00000570299.5:n.777-4402_777-4400delinsTTC
ENST00000571987.5:c.1867-27_1867-25delinsTTC ENSP00000458742.1:n.1867-27_1867-25delinsTTC
ENST00000574436.5:c.916-27_916-25delinsTTC ENSP00000460965.1:n.916-27_916-25delinsTTC
ENST00000576518.1:n.6108-27_6108-25delinsTTC
NM_001123066.3:c.1921-27_1921-25delinsTTC NP_001116538.2:n.1921-27_1921-25delinsTTC
NM_001123067.3:c.829-27_829-25delinsTTC NP_001116539.1:n.829-27_829-25delinsTTC
NM_001203251.1:c.736-27_736-25delinsTTC NP_001190180.1:n.736-27_736-25delinsTTC
NM_001203252.1:c.823-27_823-25delinsTTC NP_001190181.1:n.823-27_823-25delinsTTC
NM_005910.5:c.916-27_916-25delinsTTC NP_005901.2:n.916-27_916-25delinsTTC
NM_016834.4:c.742-27_742-25delinsTTC NP_058518.1:n.742-27_742-25delinsTTC
NM_016835.4:c.1867-27_1867-25delinsTTC NP_058519.3:n.1867-27_1867-25delinsTTC
NM_016841.4:c.649-27_649-25delinsTTC NP_058525.1:n.649-27_649-25delinsTTC
XM_005257362.3:c.2179-27_2179-25delinsTTC XP_005257419.1:n.2179-27_2179-25delinsTTC
XM_005257364.3:c.2092-27_2092-25delinsTTC XP_005257421.1:n.2092-27_2092-25delinsTTC
XM_005257365.3:c.2086-27_2086-25delinsTTC XP_005257422.1:n.2086-27_2086-25delinsTTC
XM_005257366.2:c.2005-27_2005-25delinsTTC XP_005257423.1:n.2005-27_2005-25delinsTTC
XM_005257367.3:c.1981-27_1981-25delinsTTC XP_005257424.1:n.1981-27_1981-25delinsTTC
XM_005257368.3:c.1888-27_1888-25delinsTTC XP_005257425.1:n.1888-27_1888-25delinsTTC
XM_005257369.3:c.1114-27_1114-25delinsTTC XP_005257426.1:n.1114-27_1114-25delinsTTC
XM_005257370.3:c.1027-27_1027-25delinsTTC XP_005257427.1:n.1027-27_1027-25delinsTTC
XM_005257371.3:c.940-27_940-25delinsTTC XP_005257428.1:n.940-27_940-25delinsTTC
XM_005257362.4:c.2179-27_2179-25delinsTTC XP_005257419.1:n.2179-27_2179-25delinsTTC
XM_005257364.4:c.2092-27_2092-25delinsTTC XP_005257421.1:n.2092-27_2092-25delinsTTC
XM_005257365.4:c.2086-27_2086-25delinsTTC XP_005257422.1:n.2086-27_2086-25delinsTTC
XM_005257366.3:c.2005-27_2005-25delinsTTC XP_005257423.1:n.2005-27_2005-25delinsTTC
XM_005257367.4:c.1981-27_1981-25delinsTTC XP_005257424.1:n.1981-27_1981-25delinsTTC
XM_005257368.4:c.1888-27_1888-25delinsTTC XP_005257425.1:n.1888-27_1888-25delinsTTC
XM_005257369.4:c.1114-27_1114-25delinsTTC XP_005257426.1:n.1114-27_1114-25delinsTTC
XM_005257370.4:c.1027-27_1027-25delinsTTC XP_005257427.1:n.1027-27_1027-25delinsTTC
XM_005257371.4:c.940-27_940-25delinsTTC XP_005257428.1:n.940-27_940-25delinsTTC
NM_001203251.2:c.736-27_736-25delinsTTC NP_001190180.1:n.736-27_736-25delinsTTC
NM_001377265.1:c.2092-27_2092-25delinsTTC MANE Select NP_001364194.1:n.2092-27_2092-25delinsTTC
NM_001377266.1:c.1801-27_1801-25delinsTTC NP_001364195.1:n.1801-27_1801-25delinsTTC
NM_001377267.1:c.736-27_736-25delinsTTC NP_001364196.1:n.736-27_736-25delinsTTC
NM_001377268.1:c.649-27_649-25delinsTTC NP_001364197.1:n.649-27_649-25delinsTTC
NM_016834.5:c.742-27_742-25delinsTTC NP_058518.1:n.742-27_742-25delinsTTC
NM_016841.5:c.649-27_649-25delinsTTC NP_058525.1:n.649-27_649-25delinsTTC
NR_165166.1:n.747-27_747-25delinsTTC
NM_001123066.4:c.1921-27_1921-25delinsTTC NP_001116538.2:n.1921-27_1921-25delinsTTC
NM_001123067.4:c.829-27_829-25delinsTTC NP_001116539.1:n.829-27_829-25delinsTTC
NM_001203252.2:c.823-27_823-25delinsTTC NP_001190181.1:n.823-27_823-25delinsTTC
NM_005910.6:c.916-27_916-25delinsTTC NP_005901.2:n.916-27_916-25delinsTTC
NM_016835.5:c.1867-27_1867-25delinsTTC NP_058519.3:n.1867-27_1867-25delinsTTC