Canonical Allele Identifier: CA2063449938
Gene: ALDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111791045T= , CM000674.2:g.111791045T= GRCh38
NC_000012.11:g.112228849T= , CM000674.1:g.112228849T= GRCh37
NC_000012.10:g.110713232T= NCBI36
NG_012250.1:g.29504T=
NG_012250.2:g.29159T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261733.7:c.682-261T= MANE Select ENSP00000261733.2:n.682-261T=
ENST00000546840.3:c.672-261T=
ENST00000261733.6:c.682-261T= ENSP00000261733.2:n.682-261T=
ENST00000416293.7:c.541-261T= ENSP00000403349.3:n.541-261T=
ENST00000546840.2:c.667-261T= ENSP00000450353.3:n.667-261T=
ENST00000548536.1:c.*558-261T= ENSP00000448179.1:n.*558-261T=
NM_000690.3:c.682-261T= NP_000681.2:n.682-261T=
NM_001204889.1:c.541-261T= NP_001191818.1:n.541-261T=
NM_000690.4:c.682-261T= MANE Select NP_000681.2:n.682-261T=
NM_001204889.2:c.541-261T= NP_001191818.1:n.541-261T=