Canonical Allele Identifier: CA2063464601
Gene: ALDH2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.111807502T= , CM000674.2:g.111807502T= GRCh38
NC_000012.11:g.112245306T= , CM000674.1:g.112245306T= GRCh37
NC_000012.10:g.110729689T= NCBI36
NG_012250.1:g.45961T=
NG_012250.2:g.45616T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261733.7:c.1522-2041T= MANE Select ENSP00000261733.2:n.1522-2041T=
ENST00000261733.6:c.1522-2041T= ENSP00000261733.2:n.1522-2041T=
ENST00000416293.7:c.1381-2041T= ENSP00000403349.3:n.1381-2041T=
ENST00000548536.1:c.*1398-2041T= ENSP00000448179.1:n.*1398-2041T=
ENST00000549106.1:c.453-2041T=
NM_000690.3:c.1522-2041T= NP_000681.2:n.1522-2041T=
NM_001204889.1:c.1381-2041T= NP_001191818.1:n.1381-2041T=
NM_000690.4:c.1522-2041T= MANE Select NP_000681.2:n.1522-2041T=
NM_001204889.2:c.1381-2041T= NP_001191818.1:n.1381-2041T=
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