Canonical Allele Identifier: CA358846379

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210762A>G (hg19) ; chr4:g.183289609A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289609A>G , CM000666.2:g.183289609A>G	GRCh38
NC_000004.11:g.184210762A>G , CM000666.1:g.184210762A>G	GRCh37
NC_000004.10:g.184447756A>G	NCBI36
NG_051586.1:g.195975A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3358A>G MANE Select	ENSP00000384222.3:p.Arg1120Gly
ENST00000403733.7:c.3358A>G	ENSP00000384222.3:p.Arg1120Gly
ENST00000427431.5:c.*2750A>G	ENSP00000393342.1:n.*2750A>G
ENST00000438543.5:c.*1154A>G	ENSP00000413521.1:n.*1154A>G
ENST00000448232.6:c.3430A>G	ENSP00000398577.2:p.Arg1144Gly
ENST00000504005.5:c.2404A>G	ENSP00000427569.1:p.Arg802Gly
ENST00000508747.1:c.742A>G	ENSP00000420835.1:p.Arg248Gly
ENST00000513834.5:c.3211A>G	ENSP00000425054.1:p.Arg1071Gly
NM_024949.5:c.3358A>G	NP_079225.5:p.Arg1120Gly
XM_011532269.1:c.3430A>G	XP_011530571.1:p.Arg1144Gly
XM_011532269.3:c.3430A>G	XP_011530571.1:p.Arg1144Gly
XM_024454225.1:c.3136A>G	XP_024309993.1:p.Arg1046Gly
NM_024949.6:c.3358A>G MANE Select	NP_079225.5:p.Arg1120Gly