Canonical Allele Identifier: CA357497599
Gene: ADH7 HGNC NCBI

Linked Data

COSMIC: COSM3373331 COSM3373332
MyVariant Identifiers: chr4:g.100341811A>T (hg19) chr4:g.99420654A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99420654A>T , CM000666.2:g.99420654A>T GRCh38
NC_000004.11:g.100341811A>T , CM000666.1:g.100341811A>T GRCh37
NC_000004.10:g.100560834A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437033.7:c.704T>A MANE Select ENSP00000414254.2:p.Val235Glu
ENST00000209665.8:c.740T>A ENSP00000209665.4:p.Val247Glu
ENST00000437033.6:c.704T>A ENSP00000414254.2:p.Val235Glu
ENST00000476959.5:c.764T>A ENSP00000420269.1:p.Val255Glu
ENST00000482593.5:c.533T>A ENSP00000420613.1:p.Val178Glu
NM_000673.4:c.740T>A NP_000664.2:p.Val247Glu
NM_001166504.1:c.764T>A NP_001159976.1:p.Val255Glu
NM_000673.7:c.704T>A MANE Select NP_000664.3:p.Val235Glu
NM_001166504.2:c.764T>A NP_001159976.1:p.Val255Glu
Search 100 bp 5'
Search 100 bp 3'