Canonical Allele Identifier: CA442557564

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210609T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289456T>C , CM000666.2:g.183289456T>C	GRCh38
NC_000004.11:g.184210609T>C , CM000666.1:g.184210609T>C	GRCh37
NC_000004.10:g.184447603T>C	NCBI36
NG_051586.1:g.195822T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3205T>C MANE Select	ENSP00000384222.3:p.Leu1069=
ENST00000403733.7:c.3205T>C	ENSP00000384222.3:p.Leu1069=
ENST00000427431.5:c.*2597T>C	ENSP00000393342.1:n.*2597T>C
ENST00000438543.5:c.*1001T>C	ENSP00000413521.1:n.*1001T>C
ENST00000448232.6:c.3277T>C	ENSP00000398577.2:p.Leu1093=
ENST00000504005.5:c.2251T>C	ENSP00000427569.1:p.Leu751=
ENST00000508747.1:c.589T>C	ENSP00000420835.1:p.Leu197=
ENST00000513834.5:c.3058T>C	ENSP00000425054.1:p.Leu1020=
NM_024949.5:c.3205T>C	NP_079225.5:p.Leu1069=
XM_011532269.1:c.3277T>C	XP_011530571.1:p.Leu1093=
XM_011532269.3:c.3277T>C	XP_011530571.1:p.Leu1093=
XM_024454225.1:c.2983T>C	XP_024309993.1:p.Leu995=
NM_024949.6:c.3205T>C MANE Select	NP_079225.5:p.Leu1069=