Canonical Allele Identifier: CA358845739

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210576A>T (hg19) ; chr4:g.183289423A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289423A>T , CM000666.2:g.183289423A>T	GRCh38
NC_000004.11:g.184210576A>T , CM000666.1:g.184210576A>T	GRCh37
NC_000004.10:g.184447570A>T	NCBI36
NG_051586.1:g.195789A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3172A>T MANE Select	ENSP00000384222.3:p.Thr1058Ser
ENST00000403733.7:c.3172A>T	ENSP00000384222.3:p.Thr1058Ser
ENST00000427431.5:c.*2564A>T	ENSP00000393342.1:n.*2564A>T
ENST00000438543.5:c.*968A>T	ENSP00000413521.1:n.*968A>T
ENST00000448232.6:c.3244A>T	ENSP00000398577.2:p.Thr1082Ser
ENST00000504005.5:c.2218A>T	ENSP00000427569.1:p.Thr740Ser
ENST00000508747.1:c.556A>T	ENSP00000420835.1:p.Thr186Ser
ENST00000513834.5:c.3025A>T	ENSP00000425054.1:p.Thr1009Ser
NM_024949.5:c.3172A>T	NP_079225.5:p.Thr1058Ser
XM_011532269.1:c.3244A>T	XP_011530571.1:p.Thr1082Ser
XM_011532269.3:c.3244A>T	XP_011530571.1:p.Thr1082Ser
XM_024454225.1:c.2950A>T	XP_024309993.1:p.Thr984Ser
NM_024949.6:c.3172A>T MANE Select	NP_079225.5:p.Thr1058Ser