Canonical Allele Identifier: CA2063463789

Gene: ALDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111806486C= , CM000674.2:g.111806486C=	GRCh38
NC_000012.11:g.112244290C= , CM000674.1:g.112244290C=	GRCh37
NC_000012.10:g.110728673C=	NCBI36
NG_012250.1:g.44945C=
NG_012250.2:g.44600C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261733.7:c.1521+2513C= MANE Select	ENSP00000261733.2:n.1521+2513C=
ENST00000261733.6:c.1521+2513C=	ENSP00000261733.2:n.1521+2513C=
ENST00000416293.7:c.1380+2513C=	ENSP00000403349.3:n.1380+2513C=
ENST00000548536.1:c.*1397+2513C=	ENSP00000448179.1:n.*1397+2513C=
ENST00000549106.1:c.452+2513C=
NM_000690.3:c.1521+2513C=	NP_000681.2:n.1521+2513C=
NM_001204889.1:c.1380+2513C=	NP_001191818.1:n.1380+2513C=
NM_000690.4:c.1521+2513C= MANE Select	NP_000681.2:n.1521+2513C=
NM_001204889.2:c.1380+2513C=	NP_001191818.1:n.1380+2513C=