Canonical Allele Identifier: CA442557659

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210680C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289527C>T , CM000666.2:g.183289527C>T	GRCh38
NC_000004.11:g.184210680C>T , CM000666.1:g.184210680C>T	GRCh37
NC_000004.10:g.184447674C>T	NCBI36
NG_051586.1:g.195893C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3276C>T MANE Select	ENSP00000384222.3:p.Asp1092=
ENST00000403733.7:c.3276C>T	ENSP00000384222.3:p.Asp1092=
ENST00000427431.5:c.*2668C>T	ENSP00000393342.1:n.*2668C>T
ENST00000438543.5:c.*1072C>T	ENSP00000413521.1:n.*1072C>T
ENST00000448232.6:c.3348C>T	ENSP00000398577.2:p.Asp1116=
ENST00000504005.5:c.2322C>T	ENSP00000427569.1:p.Asp774=
ENST00000508747.1:c.660C>T	ENSP00000420835.1:p.Asp220=
ENST00000513834.5:c.3129C>T	ENSP00000425054.1:p.Asp1043=
NM_024949.5:c.3276C>T	NP_079225.5:p.Asp1092=
XM_011532269.1:c.3348C>T	XP_011530571.1:p.Asp1116=
XM_011532269.3:c.3348C>T	XP_011530571.1:p.Asp1116=
XM_024454225.1:c.3054C>T	XP_024309993.1:p.Asp1018=
NM_024949.6:c.3276C>T MANE Select	NP_079225.5:p.Asp1092=