Canonical Allele Identifier: CA358845732

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210573A>T (hg19) ; chr4:g.183289420A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289420A>T , CM000666.2:g.183289420A>T	GRCh38
NC_000004.11:g.184210573A>T , CM000666.1:g.184210573A>T	GRCh37
NC_000004.10:g.184447567A>T	NCBI36
NG_051586.1:g.195786A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3169A>T MANE Select	ENSP00000384222.3:p.Thr1057Ser
ENST00000403733.7:c.3169A>T	ENSP00000384222.3:p.Thr1057Ser
ENST00000427431.5:c.*2561A>T	ENSP00000393342.1:n.*2561A>T
ENST00000438543.5:c.*965A>T	ENSP00000413521.1:n.*965A>T
ENST00000448232.6:c.3241A>T	ENSP00000398577.2:p.Thr1081Ser
ENST00000504005.5:c.2215A>T	ENSP00000427569.1:p.Thr739Ser
ENST00000508747.1:c.553A>T	ENSP00000420835.1:p.Thr185Ser
ENST00000513834.5:c.3022A>T	ENSP00000425054.1:p.Thr1008Ser
NM_024949.5:c.3169A>T	NP_079225.5:p.Thr1057Ser
XM_011532269.1:c.3241A>T	XP_011530571.1:p.Thr1081Ser
XM_011532269.3:c.3241A>T	XP_011530571.1:p.Thr1081Ser
XM_024454225.1:c.2947A>T	XP_024309993.1:p.Thr983Ser
NM_024949.6:c.3169A>T MANE Select	NP_079225.5:p.Thr1057Ser