Canonical Allele Identifier: CA386748117
Gene: ALDH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111803878T>G , CM000674.2:g.111803878T>G GRCh38
NC_000012.11:g.112241682T>G , CM000674.1:g.112241682T>G GRCh37
NC_000012.10:g.110726065T>G NCBI36
NG_012250.1:g.42337T>G
NG_012250.2:g.41992T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261733.7:c.1426T>G MANE Select ENSP00000261733.2:p.Phe476Val
ENST00000261733.6:c.1426T>G ENSP00000261733.2:p.Phe476Val
ENST00000416293.7:c.1285T>G ENSP00000403349.3:p.Phe429Val
ENST00000548536.1:c.*1302T>G ENSP00000448179.1:n.*1302T>G
ENST00000549106.1:c.357T>G
NM_000690.3:c.1426T>G NP_000681.2:p.Phe476Val
NM_001204889.1:c.1285T>G NP_001191818.1:p.Phe429Val
NM_000690.4:c.1426T>G MANE Select NP_000681.2:p.Phe476Val
NM_001204889.2:c.1285T>G NP_001191818.1:p.Phe429Val