Canonical Allele Identifier: CA442557728

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210785G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289632G>A , CM000666.2:g.183289632G>A	GRCh38
NC_000004.11:g.184210785G>A , CM000666.1:g.184210785G>A	GRCh37
NC_000004.10:g.184447779G>A	NCBI36
NG_051586.1:g.195998G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3381G>A MANE Select	ENSP00000384222.3:p.Lys1127=
ENST00000403733.7:c.3381G>A	ENSP00000384222.3:p.Lys1127=
ENST00000427431.5:c.*2773G>A	ENSP00000393342.1:n.*2773G>A
ENST00000438543.5:c.*1177G>A	ENSP00000413521.1:n.*1177G>A
ENST00000448232.6:c.3453G>A	ENSP00000398577.2:p.Lys1151=
ENST00000504005.5:c.2427G>A	ENSP00000427569.1:p.Lys809=
ENST00000508747.1:c.765G>A	ENSP00000420835.1:p.Lys255=
ENST00000513834.5:c.3234G>A	ENSP00000425054.1:p.Lys1078=
NM_024949.5:c.3381G>A	NP_079225.5:p.Lys1127=
XM_011532269.1:c.3453G>A	XP_011530571.1:p.Lys1151=
XM_011532269.3:c.3453G>A	XP_011530571.1:p.Lys1151=
XM_024454225.1:c.3159G>A	XP_024309993.1:p.Lys1053=
NM_024949.6:c.3381G>A MANE Select	NP_079225.5:p.Lys1127=