Canonical Allele Identifier: CA442557612

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210617G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289464G>C , CM000666.2:g.183289464G>C	GRCh38
NC_000004.11:g.184210617G>C , CM000666.1:g.184210617G>C	GRCh37
NC_000004.10:g.184447611G>C	NCBI36
NG_051586.1:g.195830G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3213G>C MANE Select	ENSP00000384222.3:p.Leu1071=
ENST00000403733.7:c.3213G>C	ENSP00000384222.3:p.Leu1071=
ENST00000427431.5:c.*2605G>C	ENSP00000393342.1:n.*2605G>C
ENST00000438543.5:c.*1009G>C	ENSP00000413521.1:n.*1009G>C
ENST00000448232.6:c.3285G>C	ENSP00000398577.2:p.Leu1095=
ENST00000504005.5:c.2259G>C	ENSP00000427569.1:p.Leu753=
ENST00000508747.1:c.597G>C	ENSP00000420835.1:p.Leu199=
ENST00000513834.5:c.3066G>C	ENSP00000425054.1:p.Leu1022=
NM_024949.5:c.3213G>C	NP_079225.5:p.Leu1071=
XM_011532269.1:c.3285G>C	XP_011530571.1:p.Leu1095=
XM_011532269.3:c.3285G>C	XP_011530571.1:p.Leu1095=
XM_024454225.1:c.2991G>C	XP_024309993.1:p.Leu997=
NM_024949.6:c.3213G>C MANE Select	NP_079225.5:p.Leu1071=