Canonical Allele Identifier: CA2063464899
Gene: ALDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111807876T= , CM000674.2:g.111807876T= GRCh38
NC_000012.11:g.112245680T= , CM000674.1:g.112245680T= GRCh37
NC_000012.10:g.110730063T= NCBI36
NG_012250.1:g.46335T=
NG_012250.2:g.45990T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261733.7:c.1522-1667T= MANE Select ENSP00000261733.2:n.1522-1667T=
ENST00000261733.6:c.1522-1667T= ENSP00000261733.2:n.1522-1667T=
ENST00000416293.7:c.1381-1667T= ENSP00000403349.3:n.1381-1667T=
ENST00000548536.1:c.*1398-1667T= ENSP00000448179.1:n.*1398-1667T=
ENST00000549106.1:c.453-1667T=
NM_000690.3:c.1522-1667T= NP_000681.2:n.1522-1667T=
NM_001204889.1:c.1381-1667T= NP_001191818.1:n.1381-1667T=
NM_000690.4:c.1522-1667T= MANE Select NP_000681.2:n.1522-1667T=
NM_001204889.2:c.1381-1667T= NP_001191818.1:n.1381-1667T=