Canonical Allele Identifier: CA2063464859

Gene: ALDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.111807847_111807848delinsAT , CM000674.2:g.111807847_111807848delinsAT	GRCh38
NC_000012.11:g.112245651_112245652delinsAT , CM000674.1:g.112245651_112245652delinsAT	GRCh37
NC_000012.10:g.110730034_110730035delinsAT	NCBI36
NG_012250.1:g.46306_46307delinsAT
NG_012250.2:g.45961_45962delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000261733.7:c.1522-1696_1522-1695delinsAT MANE Select	ENSP00000261733.2:n.1522-1696_1522-1695delinsAT
ENST00000261733.6:c.1522-1696_1522-1695delinsAT	ENSP00000261733.2:n.1522-1696_1522-1695delinsAT
ENST00000416293.7:c.1381-1696_1381-1695delinsAT	ENSP00000403349.3:n.1381-1696_1381-1695delinsAT
ENST00000548536.1:c.*1398-1696_*1398-1695delinsAT	ENSP00000448179.1:n.*1398-1696_*1398-1695delinsAT
ENST00000549106.1:c.453-1696_453-1695delinsAT
NM_000690.3:c.1522-1696_1522-1695delinsAT	NP_000681.2:n.1522-1696_1522-1695delinsAT
NM_001204889.1:c.1381-1696_1381-1695delinsAT	NP_001191818.1:n.1381-1696_1381-1695delinsAT
NM_000690.4:c.1522-1696_1522-1695delinsAT MANE Select	NP_000681.2:n.1522-1696_1522-1695delinsAT
NM_001204889.2:c.1381-1696_1381-1695delinsAT	NP_001191818.1:n.1381-1696_1381-1695delinsAT