Canonical Allele Identifier: CA14404041
Gene: MAPT HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs17650991

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.45967142A>C , CM000679.2:g.45967142A>C GRCh38
NC_000017.10:g.44044508A>C , CM000679.1:g.44044508A>C GRCh37
NC_000017.9:g.41400344A>C NCBI36
NG_007398.1:g.77721A>C

Transcript Alleles

HGVS Amino-acid change
NM_001123066.3:c.133+4672A>C VV NP_001116538.2:p.=
NM_001123067.3:c.133+4672A>C VV NP_001116539.1:p.=
NM_001203251.1:c.133+4672A>C VV NP_001190180.1:p.=
NM_001203252.1:c.133+4672A>C VV NP_001190181.1:p.=
NM_005910.5:c.133+4672A>C VV NP_005901.2:p.=
NM_016834.4:c.133+4672A>C VV NP_058518.1:p.=
NM_016835.4:c.133+4672A>C VV NP_058519.3:p.=
NM_016841.4:c.133+4672A>C VV NP_058525.1:p.=
XM_005257362.3:c.133+4672A>C XP_005257419.1:p.=
XM_005257364.3:c.133+4672A>C XP_005257421.1:p.=
XM_005257365.3:c.133+4672A>C XP_005257422.1:p.=
XM_005257366.2:c.133+4672A>C XP_005257423.1:p.=
XM_005257367.3:c.133+4672A>C XP_005257424.1:p.=
XM_005257368.3:c.133+4672A>C XP_005257425.1:p.=
XM_005257369.3:c.133+4672A>C XP_005257426.1:p.=
XM_005257370.3:c.133+4672A>C XP_005257427.1:p.=
XM_005257371.3:c.133+4672A>C XP_005257428.1:p.=
XM_005257362.4:c.133+4672A>C XP_005257419.1:p.=
XM_005257364.4:c.133+4672A>C XP_005257421.1:p.=
XM_005257365.4:c.133+4672A>C XP_005257422.1:p.=
XM_005257366.3:c.133+4672A>C XP_005257423.1:p.=
XM_005257367.4:c.133+4672A>C XP_005257424.1:p.=
XM_005257368.4:c.133+4672A>C XP_005257425.1:p.=
XM_005257369.4:c.133+4672A>C XP_005257426.1:p.=
XM_005257370.4:c.133+4672A>C XP_005257427.1:p.=
XM_005257371.4:c.133+4672A>C XP_005257428.1:p.=
ENST00000262410.9:c.133+4672A>C ENSP00000262410.5:p.=
ENST00000334239.12:c.133+4672A>C ENSP00000334886.8:p.=
ENST00000340799.9:c.133+4672A>C ENSP00000340438.5:p.=
ENST00000344290.9:c.133+4672A>C ENSP00000340820.5:p.=
ENST00000351559.9:c.133+4672A>C ENSP00000303214.7:p.=
ENST00000415613.6:n.133+4672A>C ENSP00000410838.2:p.=
ENST00000420682.6:n.133+4672A>C ENSP00000413056.2:p.=
ENST00000431008.7:n.133+4672A>C ENSP00000389250.3:p.=
ENST00000446361.7:c.133+4672A>C ENSP00000408975.3:p.=
ENST00000535772.5:c.133+4672A>C ENSP00000443028.1:p.=
ENST00000570299.5:n.261+4672A>C
ENST00000571311.5:c.134-2023A>C ENSP00000460048.1:p.=
ENST00000571987.5:n.133+4672A>C ENSP00000458742.1:p.=
ENST00000574436.5:n.133+4672A>C ENSP00000460965.1:p.=