Canonical Allele Identifier: CA2063461283
Gene: ALDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111803877G= , CM000674.2:g.111803877G= GRCh38
NC_000012.11:g.112241681G= , CM000674.1:g.112241681G= GRCh37
NC_000012.10:g.110726064G= NCBI36
NG_012250.1:g.42336G=
NG_012250.2:g.41991G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261733.7:c.1425G= MANE Select ENSP00000261733.2:p.Val475=
ENST00000261733.6:c.1425G= ENSP00000261733.2:p.Val475=
ENST00000416293.7:c.1284G= ENSP00000403349.3:p.Val428=
ENST00000548536.1:c.*1301G= ENSP00000448179.1:n.*1301G=
ENST00000549106.1:c.356G=
NM_000690.3:c.1425G= NP_000681.2:p.Val475=
NM_001204889.1:c.1284G= NP_001191818.1:p.Val428=
NM_000690.4:c.1425G= MANE Select NP_000681.2:p.Val475=
NM_001204889.2:c.1284G= NP_001191818.1:p.Val428=