Canonical Allele Identifier: CA2262104758
Community Standard Title: NM_001377265.1(MAPT):c.2282A= (p.Lys761=)
Gene: MAPT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46018726A= , CM000679.2:g.46018726A= GRCh38
NC_000017.10:g.44096092A= , CM000679.1:g.44096092A= GRCh37
NC_000017.9:g.41451939A= NCBI36
NG_007398.1:g.129316A=
NG_007398.2:g.129264A=

Transcript Alleles

HGVS Amino-acid Change
NM_001377265.1:c.2282A= MANE Select NP_001364194.1:p.Lys761=
ENST00000262410.10:c.2282A= MANE Select ENSP00000262410.6:p.Lys761=
NM_001123066.3:c.2111A= NP_001116538.2:p.Lys704=
NM_001123066.4:c.2111A= NP_001116538.2:p.Lys704=
NM_001123067.3:c.1019A= NP_001116539.1:p.Lys340=
NM_001123067.4:c.1019A= NP_001116539.1:p.Lys340=
NM_001203251.1:c.926A= NP_001190180.1:p.Lys309=
NM_001203251.2:c.926A= NP_001190180.1:p.Lys309=
NM_001203252.1:c.1013A= NP_001190181.1:p.Lys338=
NM_001203252.2:c.1013A= NP_001190181.1:p.Lys338=
NM_001377266.1:c.1991A= NP_001364195.1:p.Lys664=
NM_001377267.1:c.771+4448A= NP_001364196.1:n.771+4448A=
NM_001377268.1:c.839A= NP_001364197.1:p.Lys280=
NM_005910.5:c.1106A= NP_005901.2:p.Lys369=
NM_005910.6:c.1106A= NP_005901.2:p.Lys369=
NM_016834.4:c.932A= NP_058518.1:p.Lys311=
NM_016834.5:c.932A= NP_058518.1:p.Lys311=
NM_016835.4:c.2057A= NP_058519.3:p.Lys686=
NM_016835.5:c.2057A= NP_058519.3:p.Lys686=
NM_016841.4:c.839A= NP_058525.1:p.Lys280=
NM_016841.5:c.839A= NP_058525.1:p.Lys280=
NR_165166.1:n.937A=
ENST00000262410.9:c.2057A= ENSP00000262410.5:p.Lys686=
ENST00000334239.12:c.839A= ENSP00000334886.8:p.Lys280=
ENST00000340799.9:c.1019A= ENSP00000340438.5:p.Lys340=
ENST00000344290.10:c.1991A= ENSP00000340820.6:p.Lys664=
ENST00000344290.9:c.2111A= ENSP00000340820.5:p.Lys704=
ENST00000351559.10:c.1106A= ENSP00000303214.7:p.Lys369=
ENST00000351559.9:c.1106A= ENSP00000303214.7:p.Lys369=
ENST00000415613.6:c.2111A= ENSP00000410838.2:p.Lys704=
ENST00000420682.6:c.1019A= ENSP00000413056.2:p.Lys340=
ENST00000420682.7:c.1019A= ENSP00000413056.2:p.Lys340=
ENST00000431008.7:c.1013A= ENSP00000389250.3:p.Lys338=
ENST00000446361.7:c.932A= ENSP00000408975.3:p.Lys311=
ENST00000535772.5:c.1013A= ENSP00000443028.1:p.Lys338=
ENST00000535772.6:c.926A= ENSP00000443028.2:p.Lys309=
ENST00000570299.5:n.885A=
ENST00000571987.5:c.2057A= ENSP00000458742.1:p.Lys686=
ENST00000574436.5:c.1106A= ENSP00000460965.1:p.Lys369=
ENST00000576518.1:n.6298A=
ENST00000680542.1:c.1019A= ENSP00000505258.1:p.Lys340=
ENST00000680674.1:c.1055A= ENSP00000505478.1:p.Lys352=
ENST00000703922.1:c.1019A= ENSP00000515557.1:p.Lys340=
ENST00000703923.1:c.932A= ENSP00000515558.1:p.Lys311=
ENST00000703924.1:c.1019A= ENSP00000515559.1:p.Lys340=
ENST00000703978.1:c.1106A= ENSP00000515600.1:p.Lys369=
ENST00000703980.1:n.332A=
ENST00000703981.1:n.290A=
ENST00000703982.1:n.524A=
XM_005257362.3:c.2369A= XP_005257419.1:p.Lys790=
XM_005257362.4:c.2369A= XP_005257419.1:p.Lys790=
XM_005257364.3:c.2282A= XP_005257421.1:p.Lys761=
XM_005257364.4:c.2282A= XP_005257421.1:p.Lys761=
XM_005257365.3:c.2276A= XP_005257422.1:p.Lys759=
XM_005257365.4:c.2276A= XP_005257422.1:p.Lys759=
XM_005257366.2:c.2195A= XP_005257423.1:p.Lys732=
XM_005257366.3:c.2195A= XP_005257423.1:p.Lys732=
XM_005257367.3:c.2171A= XP_005257424.1:p.Lys724=
XM_005257367.4:c.2171A= XP_005257424.1:p.Lys724=
XM_005257368.3:c.2078A= XP_005257425.1:p.Lys693=
XM_005257368.4:c.2078A= XP_005257425.1:p.Lys693=
XM_005257369.3:c.1304A= XP_005257426.1:p.Lys435=
XM_005257369.4:c.1304A= XP_005257426.1:p.Lys435=
XM_005257370.3:c.1217A= XP_005257427.1:p.Lys406=
XM_005257370.4:c.1217A= XP_005257427.1:p.Lys406=
XM_005257371.3:c.1130A= XP_005257428.1:p.Lys377=
XM_005257371.4:c.1130A= XP_005257428.1:p.Lys377=