Canonical Allele Identifier: CA358846295

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210721C>G (hg19) ; chr4:g.183289568C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289568C>G , CM000666.2:g.183289568C>G	GRCh38
NC_000004.11:g.184210721C>G , CM000666.1:g.184210721C>G	GRCh37
NC_000004.10:g.184447715C>G	NCBI36
NG_051586.1:g.195934C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3317C>G MANE Select	ENSP00000384222.3:p.Thr1106Ser
ENST00000403733.7:c.3317C>G	ENSP00000384222.3:p.Thr1106Ser
ENST00000427431.5:c.*2709C>G	ENSP00000393342.1:n.*2709C>G
ENST00000438543.5:c.*1113C>G	ENSP00000413521.1:n.*1113C>G
ENST00000448232.6:c.3389C>G	ENSP00000398577.2:p.Thr1130Ser
ENST00000504005.5:c.2363C>G	ENSP00000427569.1:p.Thr788Ser
ENST00000508747.1:c.701C>G	ENSP00000420835.1:p.Thr234Ser
ENST00000513834.5:c.3170C>G	ENSP00000425054.1:p.Thr1057Ser
NM_024949.5:c.3317C>G	NP_079225.5:p.Thr1106Ser
XM_011532269.1:c.3389C>G	XP_011530571.1:p.Thr1130Ser
XM_011532269.3:c.3389C>G	XP_011530571.1:p.Thr1130Ser
XM_024454225.1:c.3095C>G	XP_024309993.1:p.Thr1032Ser
NM_024949.6:c.3317C>G MANE Select	NP_079225.5:p.Thr1106Ser