Canonical Allele Identifier: CA358845805

Gene: WWC2

Linked Data

• gnomAD v4: 4-183289439-T-G
• MyVariant Identifiers: chr4:g.184210592T>G (hg19) ; chr4:g.183289439T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289439T>G , CM000666.2:g.183289439T>G	GRCh38
NC_000004.11:g.184210592T>G , CM000666.1:g.184210592T>G	GRCh37
NC_000004.10:g.184447586T>G	NCBI36
NG_051586.1:g.195805T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3188T>G MANE Select	ENSP00000384222.3:p.Val1063Gly
ENST00000403733.7:c.3188T>G	ENSP00000384222.3:p.Val1063Gly
ENST00000427431.5:c.*2580T>G	ENSP00000393342.1:n.*2580T>G
ENST00000438543.5:c.*984T>G	ENSP00000413521.1:n.*984T>G
ENST00000448232.6:c.3260T>G	ENSP00000398577.2:p.Val1087Gly
ENST00000504005.5:c.2234T>G	ENSP00000427569.1:p.Val745Gly
ENST00000508747.1:c.572T>G	ENSP00000420835.1:p.Val191Gly
ENST00000513834.5:c.3041T>G	ENSP00000425054.1:p.Val1014Gly
NM_024949.5:c.3188T>G	NP_079225.5:p.Val1063Gly
XM_011532269.1:c.3260T>G	XP_011530571.1:p.Val1087Gly
XM_011532269.3:c.3260T>G	XP_011530571.1:p.Val1087Gly
XM_024454225.1:c.2966T>G	XP_024309993.1:p.Val989Gly
NM_024949.6:c.3188T>G MANE Select	NP_079225.5:p.Val1063Gly