Canonical Allele Identifier: CA2262106937
Gene: MAPT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46024061C= , CM000679.2:g.46024061C= GRCh38
NC_000017.10:g.44101427C= , CM000679.1:g.44101427C= GRCh37
NC_000017.9:g.41457272C= NCBI36
NG_007398.1:g.134649C=
NG_007398.2:g.134599C=

Transcript Alleles

HGVS Amino-acid Change
NM_001377265.1:c.2392C= MANE Select NP_001364194.1:p.Arg798=
ENST00000262410.10:c.2392C= MANE Select ENSP00000262410.6:p.Arg798=
NM_001123066.3:c.2221C= NP_001116538.2:p.Arg741=
NM_001123066.4:c.2221C= NP_001116538.2:p.Arg741=
NM_001123067.3:c.1129C= NP_001116539.1:p.Arg377=
NM_001123067.4:c.1129C= NP_001116539.1:p.Arg377=
NM_001203251.1:c.1036C= NP_001190180.1:p.Arg346=
NM_001203251.2:c.1036C= NP_001190180.1:p.Arg346=
NM_001203252.1:c.1123C= NP_001190181.1:p.Arg375=
NM_001203252.2:c.1123C= NP_001190181.1:p.Arg375=
NM_001377266.1:c.2101C= NP_001364195.1:p.Arg701=
NM_001377267.1:c.772-1056C= NP_001364196.1:n.772-1056C=
NM_001377268.1:c.949C= NP_001364197.1:p.Arg317=
NM_005910.5:c.1216C= NP_005901.2:p.Arg406=
NM_005910.6:c.1216C= NP_005901.2:p.Arg406=
NM_016834.4:c.1042C= NP_058518.1:p.Arg348=
NM_016834.5:c.1042C= NP_058518.1:p.Arg348=
NM_016835.4:c.2167C= NP_058519.3:p.Arg723=
NM_016835.5:c.2167C= NP_058519.3:p.Arg723=
NM_016841.4:c.949C= NP_058525.1:p.Arg317=
NM_016841.5:c.949C= NP_058525.1:p.Arg317=
NR_165166.1:n.1047C=
ENST00000262410.9:c.2167C= ENSP00000262410.5:p.Arg723=
ENST00000334239.12:c.949C= ENSP00000334886.8:p.Arg317=
ENST00000340799.9:c.1129C= ENSP00000340438.5:p.Arg377=
ENST00000344290.10:c.2101C= ENSP00000340820.6:p.Arg701=
ENST00000344290.9:c.2221C= ENSP00000340820.5:p.Arg741=
ENST00000351559.10:c.1216C= ENSP00000303214.7:p.Arg406=
ENST00000351559.9:c.1216C= ENSP00000303214.7:p.Arg406=
ENST00000415613.6:c.2221C= ENSP00000410838.2:p.Arg741=
ENST00000420682.6:c.1129C= ENSP00000413056.2:p.Arg377=
ENST00000420682.7:c.1129C= ENSP00000413056.2:p.Arg377=
ENST00000431008.7:c.1123C= ENSP00000389250.3:p.Arg375=
ENST00000446361.7:c.1042C= ENSP00000408975.3:p.Arg348=
ENST00000535772.5:c.1123C= ENSP00000443028.1:p.Arg375=
ENST00000535772.6:c.1036C= ENSP00000443028.2:p.Arg346=
ENST00000571987.5:c.2167C= ENSP00000458742.1:p.Arg723=
ENST00000574436.5:c.1216C= ENSP00000460965.1:p.Arg406=
ENST00000576518.1:n.6408C=
ENST00000680542.1:c.1129C= ENSP00000505258.1:p.Arg377=
ENST00000680674.1:c.1165C= ENSP00000505478.1:p.Arg389=
ENST00000703922.1:c.1129C= ENSP00000515557.1:p.Arg377=
ENST00000703923.1:c.1042C= ENSP00000515558.1:p.Arg348=
ENST00000703924.1:c.1129C= ENSP00000515559.1:p.Arg377=
ENST00000703978.1:c.1216C= ENSP00000515600.1:p.Arg406=
ENST00000703980.1:n.442C=
ENST00000703981.1:n.400C=
ENST00000703982.1:n.634C=
XM_005257362.3:c.2479C= XP_005257419.1:p.Arg827=
XM_005257362.4:c.2479C= XP_005257419.1:p.Arg827=
XM_005257364.3:c.2392C= XP_005257421.1:p.Arg798=
XM_005257364.4:c.2392C= XP_005257421.1:p.Arg798=
XM_005257365.3:c.2386C= XP_005257422.1:p.Arg796=
XM_005257365.4:c.2386C= XP_005257422.1:p.Arg796=
XM_005257366.2:c.2305C= XP_005257423.1:p.Arg769=
XM_005257366.3:c.2305C= XP_005257423.1:p.Arg769=
XM_005257367.3:c.2281C= XP_005257424.1:p.Arg761=
XM_005257367.4:c.2281C= XP_005257424.1:p.Arg761=
XM_005257368.3:c.2188C= XP_005257425.1:p.Arg730=
XM_005257368.4:c.2188C= XP_005257425.1:p.Arg730=
XM_005257369.3:c.1414C= XP_005257426.1:p.Arg472=
XM_005257369.4:c.1414C= XP_005257426.1:p.Arg472=
XM_005257370.3:c.1327C= XP_005257427.1:p.Arg443=
XM_005257370.4:c.1327C= XP_005257427.1:p.Arg443=
XM_005257371.3:c.1240C= XP_005257428.1:p.Arg414=
XM_005257371.4:c.1240C= XP_005257428.1:p.Arg414=