Canonical Allele Identifier: CA357497446
Gene: ADH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420579T>G , CM000666.2:g.99420579T>G GRCh38
NC_000004.11:g.100341736T>G , CM000666.1:g.100341736T>G GRCh37
NC_000004.10:g.100560759T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.779A>C MANE Select ENSP00000414254.2:p.Asn260Thr
ENST00000209665.8:c.815A>C ENSP00000209665.4:p.Asn272Thr
ENST00000437033.6:c.779A>C ENSP00000414254.2:p.Asn260Thr
ENST00000476959.5:c.839A>C ENSP00000420269.1:p.Asn280Thr
ENST00000482593.5:c.608A>C ENSP00000420613.1:p.Asn203Thr
NM_000673.4:c.815A>C NP_000664.2:p.Asn272Thr
NM_001166504.1:c.839A>C NP_001159976.1:p.Asn280Thr
NM_000673.7:c.779A>C MANE Select NP_000664.3:p.Asn260Thr
NM_001166504.2:c.839A>C NP_001159976.1:p.Asn280Thr