Canonical Allele Identifier: CA2262102721
Gene: MAPT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46014290G= , CM000679.2:g.46014290G= GRCh38
NC_000017.10:g.44091656G= , CM000679.1:g.44091656G= GRCh37
NC_000017.9:g.41447493G= NCBI36
NG_007398.1:g.124870G=
NG_007398.2:g.124828G=

Transcript Alleles

HGVS Amino-acid change
ENST00000420682.7:c.876G= ENSP00000413056.2:p.Lys292=
ENST00000703922.1:c.876G= ENSP00000515557.1:p.Lys292=
ENST00000703923.1:c.789G= ENSP00000515558.1:p.Lys263=
ENST00000703924.1:c.876G= ENSP00000515559.1:p.Lys292=
ENST00000703978.1:c.963G= ENSP00000515600.1:p.Lys321=
ENST00000703979.1:n.734G=
ENST00000703980.1:n.189G=
ENST00000703981.1:n.132G=
ENST00000262410.10:c.2139G= MANE Select ENSP00000262410.6:p.Lys713=
ENST00000344290.10:c.1848G= ENSP00000340820.6:p.Lys616=
ENST00000351559.10:c.963G= ENSP00000303214.7:p.Lys321=
ENST00000535772.6:c.783G= ENSP00000443028.2:p.Lys261=
ENST00000680542.1:c.876G= ENSP00000505258.1:p.Lys292=
ENST00000680674.1:c.789G= ENSP00000505478.1:p.Lys263=
ENST00000262410.9:c.1914G= ENSP00000262410.5:p.Lys638=
ENST00000334239.12:c.696G= ENSP00000334886.8:p.Lys232=
ENST00000340799.9:c.876G= ENSP00000340438.5:p.Lys292=
ENST00000344290.9:c.1968G= ENSP00000340820.5:p.Lys656=
ENST00000351559.9:c.963G= ENSP00000303214.7:p.Lys321=
ENST00000415613.6:c.1968G= ENSP00000410838.2:p.Lys656=
ENST00000420682.6:c.876G= ENSP00000413056.2:p.Lys292=
ENST00000431008.7:c.870G= ENSP00000389250.3:p.Lys290=
ENST00000446361.7:c.789G= ENSP00000408975.3:p.Lys263=
ENST00000535772.5:c.870G= ENSP00000443028.1:p.Lys290=
ENST00000570299.5:n.777-4328G=
ENST00000571987.5:c.1914G= ENSP00000458742.1:p.Lys638=
ENST00000574436.5:c.963G= ENSP00000460965.1:p.Lys321=
ENST00000576518.1:n.6155G=
NM_001123066.3:c.1968G= NP_001116538.2:p.Lys656=
NM_001123067.3:c.876G= NP_001116539.1:p.Lys292=
NM_001203251.1:c.783G= NP_001190180.1:p.Lys261=
NM_001203252.1:c.870G= NP_001190181.1:p.Lys290=
NM_005910.5:c.963G= NP_005901.2:p.Lys321=
NM_016834.4:c.789G= NP_058518.1:p.Lys263=
NM_016835.4:c.1914G= NP_058519.3:p.Lys638=
NM_016841.4:c.696G= NP_058525.1:p.Lys232=
XM_005257362.3:c.2226G= XP_005257419.1:p.Lys742=
XM_005257364.3:c.2139G= XP_005257421.1:p.Lys713=
XM_005257365.3:c.2133G= XP_005257422.1:p.Lys711=
XM_005257366.2:c.2052G= XP_005257423.1:p.Lys684=
XM_005257367.3:c.2028G= XP_005257424.1:p.Lys676=
XM_005257368.3:c.1935G= XP_005257425.1:p.Lys645=
XM_005257369.3:c.1161G= XP_005257426.1:p.Lys387=
XM_005257370.3:c.1074G= XP_005257427.1:p.Lys358=
XM_005257371.3:c.987G= XP_005257428.1:p.Lys329=
XM_005257362.4:c.2226G= XP_005257419.1:p.Lys742=
XM_005257364.4:c.2139G= XP_005257421.1:p.Lys713=
XM_005257365.4:c.2133G= XP_005257422.1:p.Lys711=
XM_005257366.3:c.2052G= XP_005257423.1:p.Lys684=
XM_005257367.4:c.2028G= XP_005257424.1:p.Lys676=
XM_005257368.4:c.1935G= XP_005257425.1:p.Lys645=
XM_005257369.4:c.1161G= XP_005257426.1:p.Lys387=
XM_005257370.4:c.1074G= XP_005257427.1:p.Lys358=
XM_005257371.4:c.987G= XP_005257428.1:p.Lys329=
NM_001203251.2:c.783G= NP_001190180.1:p.Lys261=
NM_001377265.1:c.2139G= MANE Select NP_001364194.1:p.Lys713=
NM_001377266.1:c.1848G= NP_001364195.1:p.Lys616=
NM_001377267.1:c.771+12G= NP_001364196.1:n.771+12G=
NM_001377268.1:c.696G= NP_001364197.1:p.Lys232=
NM_016834.5:c.789G= NP_058518.1:p.Lys263=
NM_016841.5:c.696G= NP_058525.1:p.Lys232=
NR_165166.1:n.794G=
NM_001123066.4:c.1968G= NP_001116538.2:p.Lys656=
NM_001123067.4:c.876G= NP_001116539.1:p.Lys292=
NM_001203252.2:c.870G= NP_001190181.1:p.Lys290=
NM_005910.6:c.963G= NP_005901.2:p.Lys321=
NM_016835.5:c.1914G= NP_058519.3:p.Lys638=