Canonical Allele Identifier: CA357497697

Gene: ADH7

Linked Data

• MyVariant Identifiers: chr4:g.100341856A>C (hg19) ; chr4:g.99420699A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99420699A>C , CM000666.2:g.99420699A>C	GRCh38
NC_000004.11:g.100341856A>C , CM000666.1:g.100341856A>C	GRCh37
NC_000004.10:g.100560879A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000437033.7:c.659T>G MANE Select	ENSP00000414254.2:p.Ile220Ser
ENST00000209665.8:c.695T>G	ENSP00000209665.4:p.Ile232Ser
ENST00000437033.6:c.659T>G	ENSP00000414254.2:p.Ile220Ser
ENST00000476959.5:c.719T>G	ENSP00000420269.1:p.Ile240Ser
ENST00000482593.5:c.488T>G	ENSP00000420613.1:p.Ile163Ser
NM_000673.4:c.695T>G	NP_000664.2:p.Ile232Ser
NM_001166504.1:c.719T>G	NP_001159976.1:p.Ile240Ser
NM_000673.7:c.659T>G MANE Select	NP_000664.3:p.Ile220Ser
NM_001166504.2:c.719T>G	NP_001159976.1:p.Ile240Ser