Canonical Allele Identifier: CA358845729

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210572A>C (hg19) ; chr4:g.183289419A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289419A>C , CM000666.2:g.183289419A>C	GRCh38
NC_000004.11:g.184210572A>C , CM000666.1:g.184210572A>C	GRCh37
NC_000004.10:g.184447566A>C	NCBI36
NG_051586.1:g.195785A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3168A>C MANE Select	ENSP00000384222.3:p.Arg1056Ser
ENST00000403733.7:c.3168A>C	ENSP00000384222.3:p.Arg1056Ser
ENST00000427431.5:c.*2560A>C	ENSP00000393342.1:n.*2560A>C
ENST00000438543.5:c.*964A>C	ENSP00000413521.1:n.*964A>C
ENST00000448232.6:c.3240A>C	ENSP00000398577.2:p.Arg1080Ser
ENST00000504005.5:c.2214A>C	ENSP00000427569.1:p.Arg738Ser
ENST00000508747.1:c.552A>C	ENSP00000420835.1:p.Arg184Ser
ENST00000513834.5:c.3021A>C	ENSP00000425054.1:p.Arg1007Ser
NM_024949.5:c.3168A>C	NP_079225.5:p.Arg1056Ser
XM_011532269.1:c.3240A>C	XP_011530571.1:p.Arg1080Ser
XM_011532269.3:c.3240A>C	XP_011530571.1:p.Arg1080Ser
XM_024454225.1:c.2946A>C	XP_024309993.1:p.Arg982Ser
NM_024949.6:c.3168A>C MANE Select	NP_079225.5:p.Arg1056Ser