Canonical Allele Identifier: CA358845720

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210568G>C (hg19) ; chr4:g.183289415G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289415G>C , CM000666.2:g.183289415G>C	GRCh38
NC_000004.11:g.184210568G>C , CM000666.1:g.184210568G>C	GRCh37
NC_000004.10:g.184447562G>C	NCBI36
NG_051586.1:g.195781G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3164G>C MANE Select	ENSP00000384222.3:p.Arg1055Thr
ENST00000403733.7:c.3164G>C	ENSP00000384222.3:p.Arg1055Thr
ENST00000427431.5:c.*2556G>C	ENSP00000393342.1:n.*2556G>C
ENST00000438543.5:c.*960G>C	ENSP00000413521.1:n.*960G>C
ENST00000448232.6:c.3236G>C	ENSP00000398577.2:p.Arg1079Thr
ENST00000504005.5:c.2210G>C	ENSP00000427569.1:p.Arg737Thr
ENST00000508747.1:c.548G>C	ENSP00000420835.1:p.Arg183Thr
ENST00000513834.5:c.3017G>C	ENSP00000425054.1:p.Arg1006Thr
NM_024949.5:c.3164G>C	NP_079225.5:p.Arg1055Thr
XM_011532269.1:c.3236G>C	XP_011530571.1:p.Arg1079Thr
XM_011532269.3:c.3236G>C	XP_011530571.1:p.Arg1079Thr
XM_024454225.1:c.2942G>C	XP_024309993.1:p.Arg981Thr
NM_024949.6:c.3164G>C MANE Select	NP_079225.5:p.Arg1055Thr