Canonical Allele Identifier: CA2063442982
Gene: ALDH2 HGNC NCBI

Linked Data

dbSNP Id: rs1049130260

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111776698dup , CM000674.2:g.111776698dup GRCh38
NC_000012.11:g.112214502dup , CM000674.1:g.112214502dup GRCh37
NC_000012.10:g.110698885dup NCBI36
NG_012250.1:g.15157dup
NG_012250.2:g.14812dup

Transcript Alleles

HGVS Amino-acid change
ENST00000261733.7:c.115-5220dup MANE Select ENSP00000261733.2:n.115-5220dup
ENST00000546840.3:c.105-5220dup
ENST00000261733.6:c.115-5220dup ENSP00000261733.2:n.115-5220dup
ENST00000416293.7:c.115-5220dup ENSP00000403349.3:n.115-5220dup
ENST00000546840.2:c.100-5220dup ENSP00000450353.3:n.100-5220dup
ENST00000548536.1:c.230+978dup ENSP00000448179.1:n.230+978dup
NM_000690.3:c.115-5220dup NP_000681.2:n.115-5220dup
NM_001204889.1:c.115-5220dup NP_001191818.1:n.115-5220dup
NM_000690.4:c.115-5220dup MANE Select NP_000681.2:n.115-5220dup
NM_001204889.2:c.115-5220dup NP_001191818.1:n.115-5220dup