Canonical Allele Identifier: CA357478789

Gene: ADH4

Linked Data

• dbSNP Id: rs1438535562
• gnomAD v2: 4-100047751-C-T
• gnomAD v4: 4-99126600-C-T
• COSMIC: COSM3598511
• MyVariant Identifiers: chr4:g.100047751C>T (hg19) ; chr4:g.99126600C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99126600C>T , CM000666.2:g.99126600C>T	GRCh38
NC_000004.11:g.100047751C>T , CM000666.1:g.100047751C>T	GRCh37
NC_000004.10:g.100266774C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.1112G>A MANE Select	ENSP00000265512.7:p.Gly371Glu
ENST00000265512.11:c.1112G>A	ENSP00000265512.7:p.Gly371Glu
ENST00000505590.5:c.1169G>A	ENSP00000425416.1:p.Gly390Glu
ENST00000506705.5:c.*1086G>A	ENSP00000426667.1:n.*1086G>A
ENST00000508393.5:c.1169G>A	ENSP00000424630.1:p.Gly390Glu
ENST00000509471.5:c.466G>A	ENSP00000424583.1:n.466G>A
ENST00000629236.2:c.1112G>A	ENSP00000486450.1:p.Gly371Glu
NM_000670.3:c.1112G>A	NP_000661.2:p.Gly371Glu
NM_000670.4:c.1112G>A	NP_000661.2:p.Gly371Glu
NM_001306171.1:c.1169G>A	NP_001293100.1:p.Gly390Glu
NM_001306172.1:c.1169G>A	NP_001293101.1:p.Gly390Glu
NR_037884.1:n.429-6955C>T
XR_938685.1:n.1340G>A
XR_938686.1:n.1331G>A
XR_938687.1:n.1204G>A
NM_000670.5:c.1112G>A MANE Select	NP_000661.2:p.Gly371Glu
NM_001306171.2:c.1169G>A	NP_001293100.1:p.Gly390Glu
NM_001306172.2:c.1169G>A	NP_001293101.1:p.Gly390Glu