Canonical Allele Identifier: CA442557644

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210659T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289506T>C , CM000666.2:g.183289506T>C	GRCh38
NC_000004.11:g.184210659T>C , CM000666.1:g.184210659T>C	GRCh37
NC_000004.10:g.184447653T>C	NCBI36
NG_051586.1:g.195872T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3255T>C MANE Select	ENSP00000384222.3:p.Asp1085=
ENST00000403733.7:c.3255T>C	ENSP00000384222.3:p.Asp1085=
ENST00000427431.5:c.*2647T>C	ENSP00000393342.1:n.*2647T>C
ENST00000438543.5:c.*1051T>C	ENSP00000413521.1:n.*1051T>C
ENST00000448232.6:c.3327T>C	ENSP00000398577.2:p.Asp1109=
ENST00000504005.5:c.2301T>C	ENSP00000427569.1:p.Asp767=
ENST00000508747.1:c.639T>C	ENSP00000420835.1:p.Asp213=
ENST00000513834.5:c.3108T>C	ENSP00000425054.1:p.Asp1036=
NM_024949.5:c.3255T>C	NP_079225.5:p.Asp1085=
XM_011532269.1:c.3327T>C	XP_011530571.1:p.Asp1109=
XM_011532269.3:c.3327T>C	XP_011530571.1:p.Asp1109=
XM_024454225.1:c.3033T>C	XP_024309993.1:p.Asp1011=
NM_024949.6:c.3255T>C MANE Select	NP_079225.5:p.Asp1085=