Canonical Allele Identifier: CA358846113

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210669G>C (hg19) ; chr4:g.183289516G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289516G>C , CM000666.2:g.183289516G>C	GRCh38
NC_000004.11:g.184210669G>C , CM000666.1:g.184210669G>C	GRCh37
NC_000004.10:g.184447663G>C	NCBI36
NG_051586.1:g.195882G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3265G>C MANE Select	ENSP00000384222.3:p.Ala1089Pro
ENST00000403733.7:c.3265G>C	ENSP00000384222.3:p.Ala1089Pro
ENST00000427431.5:c.*2657G>C	ENSP00000393342.1:n.*2657G>C
ENST00000438543.5:c.*1061G>C	ENSP00000413521.1:n.*1061G>C
ENST00000448232.6:c.3337G>C	ENSP00000398577.2:p.Ala1113Pro
ENST00000504005.5:c.2311G>C	ENSP00000427569.1:p.Ala771Pro
ENST00000508747.1:c.649G>C	ENSP00000420835.1:p.Ala217Pro
ENST00000513834.5:c.3118G>C	ENSP00000425054.1:p.Ala1040Pro
NM_024949.5:c.3265G>C	NP_079225.5:p.Ala1089Pro
XM_011532269.1:c.3337G>C	XP_011530571.1:p.Ala1113Pro
XM_011532269.3:c.3337G>C	XP_011530571.1:p.Ala1113Pro
XM_024454225.1:c.3043G>C	XP_024309993.1:p.Ala1015Pro
NM_024949.6:c.3265G>C MANE Select	NP_079225.5:p.Ala1089Pro