Canonical Allele Identifier: CA2063442991
Gene: ALDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111776705T= , CM000674.2:g.111776705T= GRCh38
NC_000012.11:g.112214509T= , CM000674.1:g.112214509T= GRCh37
NC_000012.10:g.110698892T= NCBI36
NG_012250.1:g.15164T=
NG_012250.2:g.14819T=

Transcript Alleles

HGVS Amino-acid change
ENST00000261733.7:c.115-5213T= MANE Select ENSP00000261733.2:n.115-5213T=
ENST00000546840.3:c.105-5213T=
ENST00000261733.6:c.115-5213T= ENSP00000261733.2:n.115-5213T=
ENST00000416293.7:c.115-5213T= ENSP00000403349.3:n.115-5213T=
ENST00000546840.2:c.100-5213T= ENSP00000450353.3:n.100-5213T=
ENST00000548536.1:c.230+985T= ENSP00000448179.1:n.230+985T=
NM_000690.3:c.115-5213T= NP_000681.2:n.115-5213T=
NM_001204889.1:c.115-5213T= NP_001191818.1:n.115-5213T=
NM_000690.4:c.115-5213T= MANE Select NP_000681.2:n.115-5213T=
NM_001204889.2:c.115-5213T= NP_001191818.1:n.115-5213T=