Canonical Allele Identifier: CA2063449962
Gene: ALDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111791082T= , CM000674.2:g.111791082T= GRCh38
NC_000012.11:g.112228886T= , CM000674.1:g.112228886T= GRCh37
NC_000012.10:g.110713269T= NCBI36
NG_012250.1:g.29541T=
NG_012250.2:g.29196T=

Transcript Alleles

HGVS Amino-acid change
ENST00000261733.7:c.682-224T= MANE Select ENSP00000261733.2:n.682-224T=
ENST00000546840.3:c.672-224T=
ENST00000261733.6:c.682-224T= ENSP00000261733.2:n.682-224T=
ENST00000416293.7:c.541-224T= ENSP00000403349.3:n.541-224T=
ENST00000546840.2:c.667-224T= ENSP00000450353.3:n.667-224T=
ENST00000548536.1:c.*558-224T= ENSP00000448179.1:n.*558-224T=
NM_000690.3:c.682-224T= NP_000681.2:n.682-224T=
NM_001204889.1:c.541-224T= NP_001191818.1:n.541-224T=
NM_000690.4:c.682-224T= MANE Select NP_000681.2:n.682-224T=
NM_001204889.2:c.541-224T= NP_001191818.1:n.541-224T=