Canonical Allele Identifier: CA358846336

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210744G>C (hg19) ; chr4:g.183289591G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289591G>C , CM000666.2:g.183289591G>C	GRCh38
NC_000004.11:g.184210744G>C , CM000666.1:g.184210744G>C	GRCh37
NC_000004.10:g.184447738G>C	NCBI36
NG_051586.1:g.195957G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3340G>C MANE Select	ENSP00000384222.3:p.Glu1114Gln
ENST00000403733.7:c.3340G>C	ENSP00000384222.3:p.Glu1114Gln
ENST00000427431.5:c.*2732G>C	ENSP00000393342.1:n.*2732G>C
ENST00000438543.5:c.*1136G>C	ENSP00000413521.1:n.*1136G>C
ENST00000448232.6:c.3412G>C	ENSP00000398577.2:p.Glu1138Gln
ENST00000504005.5:c.2386G>C	ENSP00000427569.1:p.Glu796Gln
ENST00000508747.1:c.724G>C	ENSP00000420835.1:p.Glu242Gln
ENST00000513834.5:c.3193G>C	ENSP00000425054.1:p.Glu1065Gln
NM_024949.5:c.3340G>C	NP_079225.5:p.Glu1114Gln
XM_011532269.1:c.3412G>C	XP_011530571.1:p.Glu1138Gln
XM_011532269.3:c.3412G>C	XP_011530571.1:p.Glu1138Gln
XM_024454225.1:c.3118G>C	XP_024309993.1:p.Glu1040Gln
NM_024949.6:c.3340G>C MANE Select	NP_079225.5:p.Glu1114Gln