Canonical Allele Identifier: CA2063461447
Gene: ALDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111803962G= , CM000674.2:g.111803962G= GRCh38
NC_000012.11:g.112241766G= , CM000674.1:g.112241766G= GRCh37
NC_000012.10:g.110726149G= NCBI36
NG_012250.1:g.42421G=
NG_012250.2:g.42076G=

Transcript Alleles

HGVS Amino-acid change
ENST00000261733.7:c.1510G= MANE Select ENSP00000261733.2:p.Glu504=
ENST00000261733.6:c.1510G= ENSP00000261733.2:p.Glu504=
ENST00000416293.7:c.1369G= ENSP00000403349.3:p.Glu457=
ENST00000548536.1:c.*1386G= ENSP00000448179.1:n.*1386G=
ENST00000549106.1:c.441G=
NM_000690.3:c.1510G= NP_000681.2:p.Glu504=
NM_001204889.1:c.1369G= NP_001191818.1:p.Glu457=
NM_000690.4:c.1510G= MANE Select NP_000681.2:p.Glu504=
NM_001204889.2:c.1369G= NP_001191818.1:p.Glu457=