Canonical Allele Identifier: CA2063464598
Gene: ALDH2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111807500A= , CM000674.2:g.111807500A= GRCh38
NC_000012.11:g.112245304A= , CM000674.1:g.112245304A= GRCh37
NC_000012.10:g.110729687A= NCBI36
NG_012250.1:g.45959A=
NG_012250.2:g.45614A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261733.7:c.1522-2043A= MANE Select ENSP00000261733.2:n.1522-2043A=
ENST00000261733.6:c.1522-2043A= ENSP00000261733.2:n.1522-2043A=
ENST00000416293.7:c.1381-2043A= ENSP00000403349.3:n.1381-2043A=
ENST00000548536.1:c.*1398-2043A= ENSP00000448179.1:n.*1398-2043A=
ENST00000549106.1:c.453-2043A=
NM_000690.3:c.1522-2043A= NP_000681.2:n.1522-2043A=
NM_001204889.1:c.1381-2043A= NP_001191818.1:n.1381-2043A=
NM_000690.4:c.1522-2043A= MANE Select NP_000681.2:n.1522-2043A=
NM_001204889.2:c.1381-2043A= NP_001191818.1:n.1381-2043A=
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