Canonical Allele Identifier: CA2262106943
Gene: MAPT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46024083C= , CM000679.2:g.46024083C= GRCh38
NC_000017.10:g.44101449C= , CM000679.1:g.44101449C= GRCh37
NC_000017.9:g.41457294C= NCBI36
NG_007398.1:g.134671C=
NG_007398.2:g.134621C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000420682.7:c.1151C= ENSP00000413056.2:p.Ser384=
ENST00000703922.1:c.1151C= ENSP00000515557.1:p.Ser384=
ENST00000703923.1:c.1064C= ENSP00000515558.1:p.Ser355=
ENST00000703924.1:c.1151C= ENSP00000515559.1:p.Ser384=
ENST00000703978.1:c.1238C= ENSP00000515600.1:p.Ser413=
ENST00000703980.1:n.464C=
ENST00000703981.1:n.422C=
ENST00000703982.1:n.656C=
ENST00000262410.10:c.2414C= MANE Select ENSP00000262410.6:p.Ser805=
ENST00000344290.10:c.2123C= ENSP00000340820.6:p.Ser708=
ENST00000351559.10:c.1238C= ENSP00000303214.7:p.Ser413=
ENST00000535772.6:c.1058C= ENSP00000443028.2:p.Ser353=
ENST00000680542.1:c.1151C= ENSP00000505258.1:p.Ser384=
ENST00000680674.1:c.1187C= ENSP00000505478.1:p.Ser396=
ENST00000262410.9:c.2189C= ENSP00000262410.5:p.Ser730=
ENST00000334239.12:c.971C= ENSP00000334886.8:p.Ser324=
ENST00000340799.9:c.1151C= ENSP00000340438.5:p.Ser384=
ENST00000344290.9:c.2243C= ENSP00000340820.5:p.Ser748=
ENST00000351559.9:c.1238C= ENSP00000303214.7:p.Ser413=
ENST00000415613.6:c.2243C= ENSP00000410838.2:p.Ser748=
ENST00000420682.6:c.1151C= ENSP00000413056.2:p.Ser384=
ENST00000431008.7:c.1145C= ENSP00000389250.3:p.Ser382=
ENST00000446361.7:c.1064C= ENSP00000408975.3:p.Ser355=
ENST00000535772.5:c.1145C= ENSP00000443028.1:p.Ser382=
ENST00000571987.5:c.2189C= ENSP00000458742.1:p.Ser730=
ENST00000574436.5:c.1238C= ENSP00000460965.1:p.Ser413=
ENST00000576518.1:n.6430C=
NM_001123066.3:c.2243C= NP_001116538.2:p.Ser748=
NM_001123067.3:c.1151C= NP_001116539.1:p.Ser384=
NM_001203251.1:c.1058C= NP_001190180.1:p.Ser353=
NM_001203252.1:c.1145C= NP_001190181.1:p.Ser382=
NM_005910.5:c.1238C= NP_005901.2:p.Ser413=
NM_016834.4:c.1064C= NP_058518.1:p.Ser355=
NM_016835.4:c.2189C= NP_058519.3:p.Ser730=
NM_016841.4:c.971C= NP_058525.1:p.Ser324=
XM_005257362.3:c.2501C= XP_005257419.1:p.Ser834=
XM_005257364.3:c.2414C= XP_005257421.1:p.Ser805=
XM_005257365.3:c.2408C= XP_005257422.1:p.Ser803=
XM_005257366.2:c.2327C= XP_005257423.1:p.Ser776=
XM_005257367.3:c.2303C= XP_005257424.1:p.Ser768=
XM_005257368.3:c.2210C= XP_005257425.1:p.Ser737=
XM_005257369.3:c.1436C= XP_005257426.1:p.Ser479=
XM_005257370.3:c.1349C= XP_005257427.1:p.Ser450=
XM_005257371.3:c.1262C= XP_005257428.1:p.Ser421=
XM_005257362.4:c.2501C= XP_005257419.1:p.Ser834=
XM_005257364.4:c.2414C= XP_005257421.1:p.Ser805=
XM_005257365.4:c.2408C= XP_005257422.1:p.Ser803=
XM_005257366.3:c.2327C= XP_005257423.1:p.Ser776=
XM_005257367.4:c.2303C= XP_005257424.1:p.Ser768=
XM_005257368.4:c.2210C= XP_005257425.1:p.Ser737=
XM_005257369.4:c.1436C= XP_005257426.1:p.Ser479=
XM_005257370.4:c.1349C= XP_005257427.1:p.Ser450=
XM_005257371.4:c.1262C= XP_005257428.1:p.Ser421=
NM_001203251.2:c.1058C= NP_001190180.1:p.Ser353=
NM_001377265.1:c.2414C= MANE Select NP_001364194.1:p.Ser805=
NM_001377266.1:c.2123C= NP_001364195.1:p.Ser708=
NM_001377267.1:c.772-1034C= NP_001364196.1:n.772-1034C=
NM_001377268.1:c.971C= NP_001364197.1:p.Ser324=
NM_016834.5:c.1064C= NP_058518.1:p.Ser355=
NM_016841.5:c.971C= NP_058525.1:p.Ser324=
NR_165166.1:n.1069C=
NM_001123066.4:c.2243C= NP_001116538.2:p.Ser748=
NM_001123067.4:c.1151C= NP_001116539.1:p.Ser384=
NM_001203252.2:c.1145C= NP_001190181.1:p.Ser382=
NM_005910.6:c.1238C= NP_005901.2:p.Ser413=
NM_016835.5:c.2189C= NP_058519.3:p.Ser730=