Canonical Allele Identifier: CA440506403
Gene: ADH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.100341771T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420614T>C , CM000666.2:g.99420614T>C GRCh38
NC_000004.11:g.100341771T>C , CM000666.1:g.100341771T>C GRCh37
NC_000004.10:g.100560794T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000437033.7:c.744A>G MANE Select ENSP00000414254.2:p.Lys248=
ENST00000209665.8:c.780A>G ENSP00000209665.4:p.Lys260=
ENST00000437033.6:c.744A>G ENSP00000414254.2:p.Lys248=
ENST00000476959.5:c.804A>G ENSP00000420269.1:p.Lys268=
ENST00000482593.5:c.573A>G ENSP00000420613.1:p.Lys191=
NM_000673.4:c.780A>G NP_000664.2:p.Lys260=
NM_001166504.1:c.804A>G NP_001159976.1:p.Lys268=
NM_000673.7:c.744A>G MANE Select NP_000664.3:p.Lys248=
NM_001166504.2:c.804A>G NP_001159976.1:p.Lys268=