Canonical Allele Identifier: CA386748329
Gene: ALDH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111803964A>C , CM000674.2:g.111803964A>C GRCh38
NC_000012.11:g.112241768A>C , CM000674.1:g.112241768A>C GRCh37
NC_000012.10:g.110726151A>C NCBI36
NG_012250.1:g.42423A>C
NG_012250.2:g.42078A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261733.7:c.1512A>C MANE Select ENSP00000261733.2:p.Glu504Asp
ENST00000261733.6:c.1512A>C ENSP00000261733.2:p.Glu504Asp
ENST00000416293.7:c.1371A>C ENSP00000403349.3:p.Glu457Asp
ENST00000548536.1:c.*1388A>C ENSP00000448179.1:n.*1388A>C
ENST00000549106.1:c.443A>C
NM_000690.3:c.1512A>C NP_000681.2:p.Glu504Asp
NM_001204889.1:c.1371A>C NP_001191818.1:p.Glu457Asp
NM_000690.4:c.1512A>C MANE Select NP_000681.2:p.Glu504Asp
NM_001204889.2:c.1371A>C NP_001191818.1:p.Glu457Asp