Canonical Allele Identifier: CA358845815

Gene: WWC2

Linked Data

• gnomAD v4: 4-183289444-A-G
• MyVariant Identifiers: chr4:g.184210597A>G (hg19) ; chr4:g.183289444A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289444A>G , CM000666.2:g.183289444A>G	GRCh38
NC_000004.11:g.184210597A>G , CM000666.1:g.184210597A>G	GRCh37
NC_000004.10:g.184447591A>G	NCBI36
NG_051586.1:g.195810A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3193A>G MANE Select	ENSP00000384222.3:p.Thr1065Ala
ENST00000403733.7:c.3193A>G	ENSP00000384222.3:p.Thr1065Ala
ENST00000427431.5:c.*2585A>G	ENSP00000393342.1:n.*2585A>G
ENST00000438543.5:c.*989A>G	ENSP00000413521.1:n.*989A>G
ENST00000448232.6:c.3265A>G	ENSP00000398577.2:p.Thr1089Ala
ENST00000504005.5:c.2239A>G	ENSP00000427569.1:p.Thr747Ala
ENST00000508747.1:c.577A>G	ENSP00000420835.1:p.Thr193Ala
ENST00000513834.5:c.3046A>G	ENSP00000425054.1:p.Thr1016Ala
NM_024949.5:c.3193A>G	NP_079225.5:p.Thr1065Ala
XM_011532269.1:c.3265A>G	XP_011530571.1:p.Thr1089Ala
XM_011532269.3:c.3265A>G	XP_011530571.1:p.Thr1089Ala
XM_024454225.1:c.2971A>G	XP_024309993.1:p.Thr991Ala
NM_024949.6:c.3193A>G MANE Select	NP_079225.5:p.Thr1065Ala