Canonical Allele Identifier: CA442557637

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210647C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289494C>T , CM000666.2:g.183289494C>T	GRCh38
NC_000004.11:g.184210647C>T , CM000666.1:g.184210647C>T	GRCh37
NC_000004.10:g.184447641C>T	NCBI36
NG_051586.1:g.195860C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3243C>T MANE Select	ENSP00000384222.3:p.Ser1081=
ENST00000403733.7:c.3243C>T	ENSP00000384222.3:p.Ser1081=
ENST00000427431.5:c.*2635C>T	ENSP00000393342.1:n.*2635C>T
ENST00000438543.5:c.*1039C>T	ENSP00000413521.1:n.*1039C>T
ENST00000448232.6:c.3315C>T	ENSP00000398577.2:p.Ser1105=
ENST00000504005.5:c.2289C>T	ENSP00000427569.1:p.Ser763=
ENST00000508747.1:c.627C>T	ENSP00000420835.1:p.Ser209=
ENST00000513834.5:c.3096C>T	ENSP00000425054.1:p.Ser1032=
NM_024949.5:c.3243C>T	NP_079225.5:p.Ser1081=
XM_011532269.1:c.3315C>T	XP_011530571.1:p.Ser1105=
XM_011532269.3:c.3315C>T	XP_011530571.1:p.Ser1105=
XM_024454225.1:c.3021C>T	XP_024309993.1:p.Ser1007=
NM_024949.6:c.3243C>T MANE Select	NP_079225.5:p.Ser1081=