Canonical Allele Identifier: CA2063442941
Gene: ALDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111776565A= , CM000674.2:g.111776565A= GRCh38
NC_000012.11:g.112214369A= , CM000674.1:g.112214369A= GRCh37
NC_000012.10:g.110698752A= NCBI36
NG_012250.1:g.15024A=
NG_012250.2:g.14679A=

Transcript Alleles

HGVS Amino-acid change
ENST00000261733.7:c.115-5353A= MANE Select ENSP00000261733.2:n.115-5353A=
ENST00000546840.3:c.105-5353A=
ENST00000261733.6:c.115-5353A= ENSP00000261733.2:n.115-5353A=
ENST00000416293.7:c.115-5353A= ENSP00000403349.3:n.115-5353A=
ENST00000546840.2:c.100-5353A= ENSP00000450353.3:n.100-5353A=
ENST00000548536.1:c.230+845A= ENSP00000448179.1:n.230+845A=
NM_000690.3:c.115-5353A= NP_000681.2:n.115-5353A=
NM_001204889.1:c.115-5353A= NP_001191818.1:n.115-5353A=
NM_000690.4:c.115-5353A= MANE Select NP_000681.2:n.115-5353A=
NM_001204889.2:c.115-5353A= NP_001191818.1:n.115-5353A=