Canonical Allele Identifier: CA442557679

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210713G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289560G>A , CM000666.2:g.183289560G>A	GRCh38
NC_000004.11:g.184210713G>A , CM000666.1:g.184210713G>A	GRCh37
NC_000004.10:g.184447707G>A	NCBI36
NG_051586.1:g.195926G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3309G>A MANE Select	ENSP00000384222.3:p.Gln1103=
ENST00000403733.7:c.3309G>A	ENSP00000384222.3:p.Gln1103=
ENST00000427431.5:c.*2701G>A	ENSP00000393342.1:n.*2701G>A
ENST00000438543.5:c.*1105G>A	ENSP00000413521.1:n.*1105G>A
ENST00000448232.6:c.3381G>A	ENSP00000398577.2:p.Gln1127=
ENST00000504005.5:c.2355G>A	ENSP00000427569.1:p.Gln785=
ENST00000508747.1:c.693G>A	ENSP00000420835.1:p.Gln231=
ENST00000513834.5:c.3162G>A	ENSP00000425054.1:p.Gln1054=
NM_024949.5:c.3309G>A	NP_079225.5:p.Gln1103=
XM_011532269.1:c.3381G>A	XP_011530571.1:p.Gln1127=
XM_011532269.3:c.3381G>A	XP_011530571.1:p.Gln1127=
XM_024454225.1:c.3087G>A	XP_024309993.1:p.Gln1029=
NM_024949.6:c.3309G>A MANE Select	NP_079225.5:p.Gln1103=