Canonical Allele Identifier: CA442557511

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210566T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289413T>G , CM000666.2:g.183289413T>G	GRCh38
NC_000004.11:g.184210566T>G , CM000666.1:g.184210566T>G	GRCh37
NC_000004.10:g.184447560T>G	NCBI36
NG_051586.1:g.195779T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3162T>G MANE Select	ENSP00000384222.3:p.Leu1054=
ENST00000403733.7:c.3162T>G	ENSP00000384222.3:p.Leu1054=
ENST00000427431.5:c.*2554T>G	ENSP00000393342.1:n.*2554T>G
ENST00000438543.5:c.*958T>G	ENSP00000413521.1:n.*958T>G
ENST00000448232.6:c.3234T>G	ENSP00000398577.2:p.Leu1078=
ENST00000504005.5:c.2208T>G	ENSP00000427569.1:p.Leu736=
ENST00000508747.1:c.546T>G	ENSP00000420835.1:p.Leu182=
ENST00000513834.5:c.3015T>G	ENSP00000425054.1:p.Leu1005=
NM_024949.5:c.3162T>G	NP_079225.5:p.Leu1054=
XM_011532269.1:c.3234T>G	XP_011530571.1:p.Leu1078=
XM_011532269.3:c.3234T>G	XP_011530571.1:p.Leu1078=
XM_024454225.1:c.2940T>G	XP_024309993.1:p.Leu980=
NM_024949.6:c.3162T>G MANE Select	NP_079225.5:p.Leu1054=