Canonical Allele Identifier: CA357480077

Gene: ADH4

Linked Data

• COSMIC: COSM5400180 ; COSM5400181 ; COSM5400182
• MyVariant Identifiers: chr4:g.100048474T>A (hg19) ; chr4:g.99127323T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127323T>A , CM000666.2:g.99127323T>A	GRCh38
NC_000004.11:g.100048474T>A , CM000666.1:g.100048474T>A	GRCh37
NC_000004.10:g.100267497T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.865A>T MANE Select	ENSP00000265512.7:p.Thr289Ser
ENST00000265512.11:c.865A>T	ENSP00000265512.7:p.Thr289Ser
ENST00000505590.5:c.922A>T	ENSP00000425416.1:p.Thr308Ser
ENST00000506705.5:c.*839A>T	ENSP00000426667.1:n.*839A>T
ENST00000508393.5:c.922A>T	ENSP00000424630.1:p.Thr308Ser
ENST00000509471.5:c.334-591A>T	ENSP00000424583.1:n.334-591A>T
ENST00000629236.2:c.865A>T	ENSP00000486450.1:p.Thr289Ser
NM_000670.3:c.865A>T	NP_000661.2:p.Thr289Ser
NM_000670.4:c.865A>T	NP_000661.2:p.Thr289Ser
NM_001306171.1:c.922A>T	NP_001293100.1:p.Thr308Ser
NM_001306172.1:c.922A>T	NP_001293101.1:p.Thr308Ser
NR_037884.1:n.429-6232T>A
XR_938685.1:n.1093A>T
XR_938686.1:n.1084A>T
XR_938687.1:n.957A>T
NM_000670.5:c.865A>T MANE Select	NP_000661.2:p.Thr289Ser
NM_001306171.2:c.922A>T	NP_001293100.1:p.Thr308Ser
NM_001306172.2:c.922A>T	NP_001293101.1:p.Thr308Ser