Canonical Allele Identifier: CA2063461456
Gene: ALDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111803968A= , CM000674.2:g.111803968A= GRCh38
NC_000012.11:g.112241772A= , CM000674.1:g.112241772A= GRCh37
NC_000012.10:g.110726155A= NCBI36
NG_012250.1:g.42427A=
NG_012250.2:g.42082A=

Transcript Alleles

HGVS Amino-acid change
ENST00000261733.7:c.1516A= MANE Select ENSP00000261733.2:p.Lys506=
ENST00000261733.6:c.1516A= ENSP00000261733.2:p.Lys506=
ENST00000416293.7:c.1375A= ENSP00000403349.3:p.Lys459=
ENST00000548536.1:c.*1392A= ENSP00000448179.1:n.*1392A=
ENST00000549106.1:c.447A=
NM_000690.3:c.1516A= NP_000681.2:p.Lys506=
NM_001204889.1:c.1375A= NP_001191818.1:p.Lys459=
NM_000690.4:c.1516A= MANE Select NP_000681.2:p.Lys506=
NM_001204889.2:c.1375A= NP_001191818.1:p.Lys459=