Canonical Allele Identifier: CA357498607

Gene: ADH7

Linked Data

• MyVariant Identifiers: chr4:g.100349673C>A (hg19) ; chr4:g.99428516C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99428516C>A , CM000666.2:g.99428516C>A	GRCh38
NC_000004.11:g.100349673C>A , CM000666.1:g.100349673C>A	GRCh37
NC_000004.10:g.100568696C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000437033.7:c.235G>T MANE Select	ENSP00000414254.2:p.Glu79Ter
ENST00000209665.8:c.271G>T	ENSP00000209665.4:p.Glu91Ter
ENST00000437033.6:c.235G>T	ENSP00000414254.2:p.Glu79Ter
ENST00000474027.1:c.64G>T	ENSP00000420300.1:p.Glu22Ter
ENST00000476959.5:c.295G>T	ENSP00000420269.1:p.Glu99Ter
ENST00000482593.5:c.64G>T	ENSP00000420613.1:p.Glu22Ter
NM_000673.4:c.271G>T	NP_000664.2:p.Glu91Ter
NM_001166504.1:c.295G>T	NP_001159976.1:p.Glu99Ter
NM_000673.7:c.235G>T MANE Select	NP_000664.3:p.Glu79Ter
NM_001166504.2:c.295G>T	NP_001159976.1:p.Glu99Ter