Canonical Allele Identifier: CA2063463771
Gene: ALDH2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111806460C= , CM000674.2:g.111806460C= GRCh38
NC_000012.11:g.112244264C= , CM000674.1:g.112244264C= GRCh37
NC_000012.10:g.110728647C= NCBI36
NG_012250.1:g.44919C=
NG_012250.2:g.44574C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261733.7:c.1521+2487C= MANE Select ENSP00000261733.2:n.1521+2487C=
ENST00000261733.6:c.1521+2487C= ENSP00000261733.2:n.1521+2487C=
ENST00000416293.7:c.1380+2487C= ENSP00000403349.3:n.1380+2487C=
ENST00000548536.1:c.*1397+2487C= ENSP00000448179.1:n.*1397+2487C=
ENST00000549106.1:c.452+2487C=
NM_000690.3:c.1521+2487C= NP_000681.2:n.1521+2487C=
NM_001204889.1:c.1380+2487C= NP_001191818.1:n.1380+2487C=
NM_000690.4:c.1521+2487C= MANE Select NP_000681.2:n.1521+2487C=
NM_001204889.2:c.1380+2487C= NP_001191818.1:n.1380+2487C=
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