Canonical Allele Identifier: CA358846382

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210763G>T (hg19) ; chr4:g.183289610G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289610G>T , CM000666.2:g.183289610G>T	GRCh38
NC_000004.11:g.184210763G>T , CM000666.1:g.184210763G>T	GRCh37
NC_000004.10:g.184447757G>T	NCBI36
NG_051586.1:g.195976G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3359G>T MANE Select	ENSP00000384222.3:p.Arg1120Met
ENST00000403733.7:c.3359G>T	ENSP00000384222.3:p.Arg1120Met
ENST00000427431.5:c.*2751G>T	ENSP00000393342.1:n.*2751G>T
ENST00000438543.5:c.*1155G>T	ENSP00000413521.1:n.*1155G>T
ENST00000448232.6:c.3431G>T	ENSP00000398577.2:p.Arg1144Met
ENST00000504005.5:c.2405G>T	ENSP00000427569.1:p.Arg802Met
ENST00000508747.1:c.743G>T	ENSP00000420835.1:p.Arg248Met
ENST00000513834.5:c.3212G>T	ENSP00000425054.1:p.Arg1071Met
NM_024949.5:c.3359G>T	NP_079225.5:p.Arg1120Met
XM_011532269.1:c.3431G>T	XP_011530571.1:p.Arg1144Met
XM_011532269.3:c.3431G>T	XP_011530571.1:p.Arg1144Met
XM_024454225.1:c.3137G>T	XP_024309993.1:p.Arg1046Met
NM_024949.6:c.3359G>T MANE Select	NP_079225.5:p.Arg1120Met