Canonical Allele Identifier: CA357479983

Gene: ADH4

Linked Data

• MyVariant Identifiers: chr4:g.100048465A>G (hg19) ; chr4:g.99127314A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127314A>G , CM000666.2:g.99127314A>G	GRCh38
NC_000004.11:g.100048465A>G , CM000666.1:g.100048465A>G	GRCh37
NC_000004.10:g.100267488A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.874T>C MANE Select	ENSP00000265512.7:p.Trp292Arg
ENST00000265512.11:c.874T>C	ENSP00000265512.7:p.Trp292Arg
ENST00000505590.5:c.931T>C	ENSP00000425416.1:p.Trp311Arg
ENST00000506705.5:c.*848T>C	ENSP00000426667.1:n.*848T>C
ENST00000508393.5:c.931T>C	ENSP00000424630.1:p.Trp311Arg
ENST00000509471.5:c.334-582T>C	ENSP00000424583.1:n.334-582T>C
ENST00000629236.2:c.874T>C	ENSP00000486450.1:p.Trp292Arg
NM_000670.3:c.874T>C	NP_000661.2:p.Trp292Arg
NM_000670.4:c.874T>C	NP_000661.2:p.Trp292Arg
NM_001306171.1:c.931T>C	NP_001293100.1:p.Trp311Arg
NM_001306172.1:c.931T>C	NP_001293101.1:p.Trp311Arg
NR_037884.1:n.429-6241A>G
XR_938685.1:n.1102T>C
XR_938686.1:n.1093T>C
XR_938687.1:n.966T>C
NM_000670.5:c.874T>C MANE Select	NP_000661.2:p.Trp292Arg
NM_001306171.2:c.931T>C	NP_001293100.1:p.Trp311Arg
NM_001306172.2:c.931T>C	NP_001293101.1:p.Trp311Arg