Canonical Allele Identifier: CA358845717

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210567A>G (hg19) ; chr4:g.183289414A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289414A>G , CM000666.2:g.183289414A>G	GRCh38
NC_000004.11:g.184210567A>G , CM000666.1:g.184210567A>G	GRCh37
NC_000004.10:g.184447561A>G	NCBI36
NG_051586.1:g.195780A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3163A>G MANE Select	ENSP00000384222.3:p.Arg1055Gly
ENST00000403733.7:c.3163A>G	ENSP00000384222.3:p.Arg1055Gly
ENST00000427431.5:c.*2555A>G	ENSP00000393342.1:n.*2555A>G
ENST00000438543.5:c.*959A>G	ENSP00000413521.1:n.*959A>G
ENST00000448232.6:c.3235A>G	ENSP00000398577.2:p.Arg1079Gly
ENST00000504005.5:c.2209A>G	ENSP00000427569.1:p.Arg737Gly
ENST00000508747.1:c.547A>G	ENSP00000420835.1:p.Arg183Gly
ENST00000513834.5:c.3016A>G	ENSP00000425054.1:p.Arg1006Gly
NM_024949.5:c.3163A>G	NP_079225.5:p.Arg1055Gly
XM_011532269.1:c.3235A>G	XP_011530571.1:p.Arg1079Gly
XM_011532269.3:c.3235A>G	XP_011530571.1:p.Arg1079Gly
XM_024454225.1:c.2941A>G	XP_024309993.1:p.Arg981Gly
NM_024949.6:c.3163A>G MANE Select	NP_079225.5:p.Arg1055Gly