Canonical Allele Identifier: CA2638369808
Gene: MAPT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46014204_46014205dup , CM000679.2:g.46014204_46014205dup GRCh38
NC_000017.10:g.44091570_44091571dup , CM000679.1:g.44091570_44091571dup GRCh37
NC_000017.9:g.41447407_41447408dup NCBI36
NG_007398.1:g.124784_124785dup
NG_007398.2:g.124742_124743dup

Transcript Alleles

HGVS Amino-acid change
ENST00000420682.7:c.829-39_829-38dup ENSP00000413056.2:n.829-39_829-38dup
ENST00000703922.1:c.829-39_829-38dup ENSP00000515557.1:n.829-39_829-38dup
ENST00000703923.1:c.742-39_742-38dup ENSP00000515558.1:n.742-39_742-38dup
ENST00000703924.1:c.829-39_829-38dup ENSP00000515559.1:n.829-39_829-38dup
ENST00000703978.1:c.916-39_916-38dup ENSP00000515600.1:n.916-39_916-38dup
ENST00000703979.1:n.687-39_687-38dup
ENST00000703980.1:n.142-39_142-38dup
ENST00000703981.1:n.85-39_85-38dup
ENST00000262410.10:c.2092-39_2092-38dup MANE Select ENSP00000262410.6:n.2092-39_2092-38dup
ENST00000344290.10:c.1801-39_1801-38dup ENSP00000340820.6:n.1801-39_1801-38dup
ENST00000351559.10:c.916-39_916-38dup ENSP00000303214.7:n.916-39_916-38dup
ENST00000535772.6:c.736-39_736-38dup ENSP00000443028.2:n.736-39_736-38dup
ENST00000680542.1:c.829-39_829-38dup ENSP00000505258.1:n.829-39_829-38dup
ENST00000680674.1:c.742-39_742-38dup ENSP00000505478.1:n.742-39_742-38dup
ENST00000262410.9:c.1867-39_1867-38dup ENSP00000262410.5:n.1867-39_1867-38dup
ENST00000334239.12:c.649-39_649-38dup ENSP00000334886.8:n.649-39_649-38dup
ENST00000340799.9:c.829-39_829-38dup ENSP00000340438.5:n.829-39_829-38dup
ENST00000344290.9:c.1921-39_1921-38dup ENSP00000340820.5:n.1921-39_1921-38dup
ENST00000351559.9:c.916-39_916-38dup ENSP00000303214.7:n.916-39_916-38dup
ENST00000415613.6:c.1921-39_1921-38dup ENSP00000410838.2:n.1921-39_1921-38dup
ENST00000420682.6:c.829-39_829-38dup ENSP00000413056.2:n.829-39_829-38dup
ENST00000431008.7:c.823-39_823-38dup ENSP00000389250.3:n.823-39_823-38dup
ENST00000446361.7:c.742-39_742-38dup ENSP00000408975.3:n.742-39_742-38dup
ENST00000535772.5:c.823-39_823-38dup ENSP00000443028.1:n.823-39_823-38dup
ENST00000570299.5:n.777-4414_777-4413dup
ENST00000571987.5:c.1867-39_1867-38dup ENSP00000458742.1:n.1867-39_1867-38dup
ENST00000574436.5:c.916-39_916-38dup ENSP00000460965.1:n.916-39_916-38dup
ENST00000576518.1:n.6108-39_6108-38dup
NM_001123066.3:c.1921-39_1921-38dup NP_001116538.2:n.1921-39_1921-38dup
NM_001123067.3:c.829-39_829-38dup NP_001116539.1:n.829-39_829-38dup
NM_001203251.1:c.736-39_736-38dup NP_001190180.1:n.736-39_736-38dup
NM_001203252.1:c.823-39_823-38dup NP_001190181.1:n.823-39_823-38dup
NM_005910.5:c.916-39_916-38dup NP_005901.2:n.916-39_916-38dup
NM_016834.4:c.742-39_742-38dup NP_058518.1:n.742-39_742-38dup
NM_016835.4:c.1867-39_1867-38dup NP_058519.3:n.1867-39_1867-38dup
NM_016841.4:c.649-39_649-38dup NP_058525.1:n.649-39_649-38dup
XM_005257362.3:c.2179-39_2179-38dup XP_005257419.1:n.2179-39_2179-38dup
XM_005257364.3:c.2092-39_2092-38dup XP_005257421.1:n.2092-39_2092-38dup
XM_005257365.3:c.2086-39_2086-38dup XP_005257422.1:n.2086-39_2086-38dup
XM_005257366.2:c.2005-39_2005-38dup XP_005257423.1:n.2005-39_2005-38dup
XM_005257367.3:c.1981-39_1981-38dup XP_005257424.1:n.1981-39_1981-38dup
XM_005257368.3:c.1888-39_1888-38dup XP_005257425.1:n.1888-39_1888-38dup
XM_005257369.3:c.1114-39_1114-38dup XP_005257426.1:n.1114-39_1114-38dup
XM_005257370.3:c.1027-39_1027-38dup XP_005257427.1:n.1027-39_1027-38dup
XM_005257371.3:c.940-39_940-38dup XP_005257428.1:n.940-39_940-38dup
XM_005257362.4:c.2179-39_2179-38dup XP_005257419.1:n.2179-39_2179-38dup
XM_005257364.4:c.2092-39_2092-38dup XP_005257421.1:n.2092-39_2092-38dup
XM_005257365.4:c.2086-39_2086-38dup XP_005257422.1:n.2086-39_2086-38dup
XM_005257366.3:c.2005-39_2005-38dup XP_005257423.1:n.2005-39_2005-38dup
XM_005257367.4:c.1981-39_1981-38dup XP_005257424.1:n.1981-39_1981-38dup
XM_005257368.4:c.1888-39_1888-38dup XP_005257425.1:n.1888-39_1888-38dup
XM_005257369.4:c.1114-39_1114-38dup XP_005257426.1:n.1114-39_1114-38dup
XM_005257370.4:c.1027-39_1027-38dup XP_005257427.1:n.1027-39_1027-38dup
XM_005257371.4:c.940-39_940-38dup XP_005257428.1:n.940-39_940-38dup
NM_001203251.2:c.736-39_736-38dup NP_001190180.1:n.736-39_736-38dup
NM_001377265.1:c.2092-39_2092-38dup MANE Select NP_001364194.1:n.2092-39_2092-38dup
NM_001377266.1:c.1801-39_1801-38dup NP_001364195.1:n.1801-39_1801-38dup
NM_001377267.1:c.736-39_736-38dup NP_001364196.1:n.736-39_736-38dup
NM_001377268.1:c.649-39_649-38dup NP_001364197.1:n.649-39_649-38dup
NM_016834.5:c.742-39_742-38dup NP_058518.1:n.742-39_742-38dup
NM_016841.5:c.649-39_649-38dup NP_058525.1:n.649-39_649-38dup
NR_165166.1:n.747-39_747-38dup
NM_001123066.4:c.1921-39_1921-38dup NP_001116538.2:n.1921-39_1921-38dup
NM_001123067.4:c.829-39_829-38dup NP_001116539.1:n.829-39_829-38dup
NM_001203252.2:c.823-39_823-38dup NP_001190181.1:n.823-39_823-38dup
NM_005910.6:c.916-39_916-38dup NP_005901.2:n.916-39_916-38dup
NM_016835.5:c.1867-39_1867-38dup NP_058519.3:n.1867-39_1867-38dup