Canonical Allele Identifier: CA357479977

Gene: ADH4

Linked Data

• MyVariant Identifiers: chr4:g.100048464C>G (hg19) ; chr4:g.99127313C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127313C>G , CM000666.2:g.99127313C>G	GRCh38
NC_000004.11:g.100048464C>G , CM000666.1:g.100048464C>G	GRCh37
NC_000004.10:g.100267487C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.875G>C MANE Select	ENSP00000265512.7:p.Trp292Ser
ENST00000265512.11:c.875G>C	ENSP00000265512.7:p.Trp292Ser
ENST00000505590.5:c.932G>C	ENSP00000425416.1:p.Trp311Ser
ENST00000506705.5:c.*849G>C	ENSP00000426667.1:n.*849G>C
ENST00000508393.5:c.932G>C	ENSP00000424630.1:p.Trp311Ser
ENST00000509471.5:c.334-581G>C	ENSP00000424583.1:n.334-581G>C
ENST00000629236.2:c.875G>C	ENSP00000486450.1:p.Trp292Ser
NM_000670.3:c.875G>C	NP_000661.2:p.Trp292Ser
NM_000670.4:c.875G>C	NP_000661.2:p.Trp292Ser
NM_001306171.1:c.932G>C	NP_001293100.1:p.Trp311Ser
NM_001306172.1:c.932G>C	NP_001293101.1:p.Trp311Ser
NR_037884.1:n.429-6242C>G
XR_938685.1:n.1103G>C
XR_938686.1:n.1094G>C
XR_938687.1:n.967G>C
NM_000670.5:c.875G>C MANE Select	NP_000661.2:p.Trp292Ser
NM_001306171.2:c.932G>C	NP_001293100.1:p.Trp311Ser
NM_001306172.2:c.932G>C	NP_001293101.1:p.Trp311Ser