Canonical Allele Identifier: CA2063461465

Gene: ALDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111803977A= , CM000674.2:g.111803977A=	GRCh38
NC_000012.11:g.112241781A= , CM000674.1:g.112241781A=	GRCh37
NC_000012.10:g.110726164A=	NCBI36
NG_012250.1:g.42436A=
NG_012250.2:g.42091A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261733.7:c.1521+4A= MANE Select	ENSP00000261733.2:n.1521+4A=
ENST00000261733.6:c.1521+4A=	ENSP00000261733.2:n.1521+4A=
ENST00000416293.7:c.1380+4A=	ENSP00000403349.3:n.1380+4A=
ENST00000548536.1:c.*1397+4A=	ENSP00000448179.1:n.*1397+4A=
ENST00000549106.1:c.452+4A=
NM_000690.3:c.1521+4A=	NP_000681.2:n.1521+4A=
NM_001204889.1:c.1380+4A=	NP_001191818.1:n.1380+4A=
NM_000690.4:c.1521+4A= MANE Select	NP_000681.2:n.1521+4A=
NM_001204889.2:c.1380+4A=	NP_001191818.1:n.1380+4A=