Canonical Allele Identifier: CA358846423

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210782G>C (hg19) ; chr4:g.183289629G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289629G>C , CM000666.2:g.183289629G>C	GRCh38
NC_000004.11:g.184210782G>C , CM000666.1:g.184210782G>C	GRCh37
NC_000004.10:g.184447776G>C	NCBI36
NG_051586.1:g.195995G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3378G>C MANE Select	ENSP00000384222.3:p.Glu1126Asp
ENST00000403733.7:c.3378G>C	ENSP00000384222.3:p.Glu1126Asp
ENST00000427431.5:c.*2770G>C	ENSP00000393342.1:n.*2770G>C
ENST00000438543.5:c.*1174G>C	ENSP00000413521.1:n.*1174G>C
ENST00000448232.6:c.3450G>C	ENSP00000398577.2:p.Glu1150Asp
ENST00000504005.5:c.2424G>C	ENSP00000427569.1:p.Glu808Asp
ENST00000508747.1:c.762G>C	ENSP00000420835.1:p.Glu254Asp
ENST00000513834.5:c.3231G>C	ENSP00000425054.1:p.Glu1077Asp
NM_024949.5:c.3378G>C	NP_079225.5:p.Glu1126Asp
XM_011532269.1:c.3450G>C	XP_011530571.1:p.Glu1150Asp
XM_011532269.3:c.3450G>C	XP_011530571.1:p.Glu1150Asp
XM_024454225.1:c.3156G>C	XP_024309993.1:p.Glu1052Asp
NM_024949.6:c.3378G>C MANE Select	NP_079225.5:p.Glu1126Asp