Canonical Allele Identifier: CA8618295
Gene: MAPT HGNC NCBI

Linked Data

ClinVar Variation Id: 323650
dbSNP Id: rs9468

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46024197T>C , CM000679.2:g.46024197T>C GRCh38
NC_000017.10:g.44101563T>C , CM000679.1:g.44101563T>C GRCh37
NC_000017.9:g.41457408T>C NCBI36
NG_007398.1:g.134785T>C
NG_007398.2:g.134735T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000420682.7:c.*26T>C ENSP00000413056.2:n.*26T>C
ENST00000703922.1:c.*26T>C ENSP00000515557.1:n.*26T>C
ENST00000703923.1:c.*26T>C ENSP00000515558.1:n.*26T>C
ENST00000703924.1:c.*26T>C ENSP00000515559.1:n.*26T>C
ENST00000703978.1:c.*26T>C ENSP00000515600.1:n.*26T>C
ENST00000703980.1:n.578T>C
ENST00000703981.1:n.536T>C
ENST00000703982.1:n.770T>C
ENST00000262410.10:c.*26T>C MANE Select ENSP00000262410.6:n.*26T>C
ENST00000344290.10:c.*26T>C ENSP00000340820.6:n.*26T>C
ENST00000351559.10:c.*26T>C ENSP00000303214.7:n.*26T>C
ENST00000535772.6:c.*26T>C ENSP00000443028.2:n.*26T>C
ENST00000680542.1:c.*26T>C ENSP00000505258.1:n.*26T>C
ENST00000680674.1:c.*26T>C ENSP00000505478.1:n.*26T>C
ENST00000262410.9:c.*26T>C ENSP00000262410.5:n.*26T>C
ENST00000340799.9:c.*26T>C ENSP00000340438.5:n.*26T>C
ENST00000344290.9:c.*26T>C ENSP00000340820.5:n.*26T>C
ENST00000351559.9:c.*26T>C ENSP00000303214.7:n.*26T>C
ENST00000446361.7:c.*26T>C ENSP00000408975.3:n.*26T>C
ENST00000535772.5:c.*26T>C ENSP00000443028.1:n.*26T>C
ENST00000576518.1:n.6544T>C
NM_001123066.3:c.*26T>C NP_001116538.2:n.*26T>C
NM_001123067.3:c.*26T>C NP_001116539.1:n.*26T>C
NM_001203251.1:c.*26T>C NP_001190180.1:n.*26T>C
NM_001203252.1:c.*26T>C NP_001190181.1:n.*26T>C
NM_005910.5:c.*26T>C NP_005901.2:n.*26T>C
NM_016834.4:c.*26T>C NP_058518.1:n.*26T>C
NM_016835.4:c.*26T>C NP_058519.3:n.*26T>C
NM_016841.4:c.*26T>C NP_058525.1:n.*26T>C
XM_005257362.3:c.*26T>C XP_005257419.1:n.*26T>C
XM_005257364.3:c.*26T>C XP_005257421.1:n.*26T>C
XM_005257365.3:c.*26T>C XP_005257422.1:n.*26T>C
XM_005257366.2:c.*26T>C XP_005257423.1:n.*26T>C
XM_005257367.3:c.*26T>C XP_005257424.1:n.*26T>C
XM_005257368.3:c.*26T>C XP_005257425.1:n.*26T>C
XM_005257369.3:c.*26T>C XP_005257426.1:n.*26T>C
XM_005257370.3:c.*26T>C XP_005257427.1:n.*26T>C
XM_005257371.3:c.*26T>C XP_005257428.1:n.*26T>C
XM_005257362.4:c.*26T>C XP_005257419.1:n.*26T>C
XM_005257364.4:c.*26T>C XP_005257421.1:n.*26T>C
XM_005257365.4:c.*26T>C XP_005257422.1:n.*26T>C
XM_005257366.3:c.*26T>C XP_005257423.1:n.*26T>C
XM_005257367.4:c.*26T>C XP_005257424.1:n.*26T>C
XM_005257368.4:c.*26T>C XP_005257425.1:n.*26T>C
XM_005257369.4:c.*26T>C XP_005257426.1:n.*26T>C
XM_005257370.4:c.*26T>C XP_005257427.1:n.*26T>C
XM_005257371.4:c.*26T>C XP_005257428.1:n.*26T>C
NM_001203251.2:c.*26T>C NP_001190180.1:n.*26T>C
NM_001377265.1:c.*26T>C MANE Select NP_001364194.1:n.*26T>C
NM_001377266.1:c.*26T>C NP_001364195.1:n.*26T>C
NM_001377267.1:c.772-920T>C NP_001364196.1:n.772-920T>C
NM_001377268.1:c.*26T>C NP_001364197.1:n.*26T>C
NM_016834.5:c.*26T>C NP_058518.1:n.*26T>C
NM_016841.5:c.*26T>C NP_058525.1:n.*26T>C
NR_165166.1:n.1183T>C
NM_001123066.4:c.*26T>C NP_001116538.2:n.*26T>C
NM_001123067.4:c.*26T>C NP_001116539.1:n.*26T>C
NM_001203252.2:c.*26T>C NP_001190181.1:n.*26T>C
NM_005910.6:c.*26T>C NP_005901.2:n.*26T>C
NM_016835.5:c.*26T>C NP_058519.3:n.*26T>C