Canonical Allele Identifier: CA14379840
Gene: MAPT HGNC NCBI

Linked Data

dbSNP Id: rs2435207

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.45981562G>A , CM000679.2:g.45981562G>A GRCh38
NC_000017.10:g.44058928G>A , CM000679.1:g.44058928G>A GRCh37
NC_000017.9:g.41414765G>A NCBI36
NG_007398.1:g.92142G>A
NG_007398.2:g.92100G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262410.10:c.287-1304G>A MANE Select ENSP00000262410.6:n.287-1304G>A
ENST00000344290.10:c.287-1304G>A ENSP00000340820.6:n.287-1304G>A
ENST00000351559.10:c.373+3122G>A ENSP00000303214.7:n.373+3122G>A
ENST00000535772.6:c.286+3122G>A ENSP00000443028.2:n.286+3122G>A
ENST00000680542.1:c.286+3122G>A ENSP00000505258.1:n.286+3122G>A
ENST00000680674.1:c.199+3122G>A ENSP00000505478.1:n.199+3122G>A
ENST00000262410.9:c.374-1616G>A ENSP00000262410.5:n.374-1616G>A
ENST00000334239.12:c.199+3122G>A ENSP00000334886.8:n.199+3122G>A
ENST00000340799.9:c.286+3122G>A ENSP00000340438.5:n.286+3122G>A
ENST00000344290.9:c.374-1616G>A ENSP00000340820.5:n.374-1616G>A
ENST00000351559.9:c.373+3122G>A ENSP00000303214.7:n.373+3122G>A
ENST00000415613.6:n.374-1616G>A ENSP00000410838.2:n.374-1616G>A
ENST00000420682.6:n.286+3122G>A ENSP00000413056.2:n.286+3122G>A
ENST00000431008.7:n.373+3122G>A ENSP00000389250.3:n.373+3122G>A
ENST00000446361.7:c.199+3122G>A ENSP00000408975.3:n.199+3122G>A
ENST00000535772.5:c.373+3122G>A ENSP00000443028.1:n.373+3122G>A
ENST00000570299.5:n.327+3122G>A
ENST00000571987.5:n.374-1616G>A ENSP00000458742.1:n.374-1616G>A
ENST00000574436.5:n.373+3122G>A ENSP00000460965.1:n.373+3122G>A
ENST00000576518.1:n.5658+3122G>A
NM_001123066.3:c.374-1616G>A NP_001116538.2:n.374-1616G>A
NM_001123067.3:c.286+3122G>A NP_001116539.1:n.286+3122G>A
NM_001203251.1:c.286+3122G>A NP_001190180.1:n.286+3122G>A
NM_001203252.1:c.373+3122G>A NP_001190181.1:n.373+3122G>A
NM_005910.5:c.373+3122G>A NP_005901.2:n.373+3122G>A
NM_016834.4:c.199+3122G>A NP_058518.1:n.199+3122G>A
NM_016835.4:c.374-1616G>A NP_058519.3:n.374-1616G>A
NM_016841.4:c.199+3122G>A NP_058525.1:n.199+3122G>A
XM_005257362.3:c.374-1304G>A XP_005257419.1:n.374-1304G>A
XM_005257364.3:c.287-1304G>A XP_005257421.1:n.287-1304G>A
XM_005257365.3:c.374-1304G>A XP_005257422.1:n.374-1304G>A
XM_005257366.2:c.200-1304G>A XP_005257423.1:n.200-1304G>A
XM_005257367.3:c.374-1304G>A XP_005257424.1:n.374-1304G>A
XM_005257368.3:c.374-1304G>A XP_005257425.1:n.374-1304G>A
XM_005257369.3:c.373+3122G>A XP_005257426.1:n.373+3122G>A
XM_005257370.3:c.286+3122G>A XP_005257427.1:n.286+3122G>A
XM_005257371.3:c.199+3122G>A XP_005257428.1:n.199+3122G>A
XM_005257362.4:c.374-1304G>A XP_005257419.1:n.374-1304G>A
XM_005257364.4:c.287-1304G>A XP_005257421.1:n.287-1304G>A
XM_005257365.4:c.374-1304G>A XP_005257422.1:n.374-1304G>A
XM_005257366.3:c.200-1304G>A XP_005257423.1:n.200-1304G>A
XM_005257367.4:c.374-1304G>A XP_005257424.1:n.374-1304G>A
XM_005257368.4:c.374-1304G>A XP_005257425.1:n.374-1304G>A
XM_005257369.4:c.373+3122G>A XP_005257426.1:n.373+3122G>A
XM_005257370.4:c.286+3122G>A XP_005257427.1:n.286+3122G>A
XM_005257371.4:c.199+3122G>A XP_005257428.1:n.199+3122G>A
NM_001203251.2:c.286+3122G>A NP_001190180.1:n.286+3122G>A
NM_001377265.1:c.287-1304G>A MANE Select NP_001364194.1:n.287-1304G>A
NM_001377266.1:c.287-1304G>A NP_001364195.1:n.287-1304G>A
NM_001377267.1:c.286+3122G>A NP_001364196.1:n.286+3122G>A
NM_001377268.1:c.199+3122G>A NP_001364197.1:n.199+3122G>A
NM_016834.5:c.199+3122G>A NP_058518.1:n.199+3122G>A
NM_016841.5:c.199+3122G>A NP_058525.1:n.199+3122G>A
NR_165166.1:n.436+3122G>A
NM_001123066.4:c.374-1616G>A NP_001116538.2:n.374-1616G>A
NM_001123067.4:c.286+3122G>A NP_001116539.1:n.286+3122G>A
NM_001203252.2:c.373+3122G>A NP_001190181.1:n.373+3122G>A
NM_005910.6:c.373+3122G>A NP_005901.2:n.373+3122G>A
NM_016835.5:c.374-1616G>A NP_058519.3:n.374-1616G>A