Canonical Allele Identifier: CA358845738

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210576A>G (hg19) ; chr4:g.183289423A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289423A>G , CM000666.2:g.183289423A>G	GRCh38
NC_000004.11:g.184210576A>G , CM000666.1:g.184210576A>G	GRCh37
NC_000004.10:g.184447570A>G	NCBI36
NG_051586.1:g.195789A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3172A>G MANE Select	ENSP00000384222.3:p.Thr1058Ala
ENST00000403733.7:c.3172A>G	ENSP00000384222.3:p.Thr1058Ala
ENST00000427431.5:c.*2564A>G	ENSP00000393342.1:n.*2564A>G
ENST00000438543.5:c.*968A>G	ENSP00000413521.1:n.*968A>G
ENST00000448232.6:c.3244A>G	ENSP00000398577.2:p.Thr1082Ala
ENST00000504005.5:c.2218A>G	ENSP00000427569.1:p.Thr740Ala
ENST00000508747.1:c.556A>G	ENSP00000420835.1:p.Thr186Ala
ENST00000513834.5:c.3025A>G	ENSP00000425054.1:p.Thr1009Ala
NM_024949.5:c.3172A>G	NP_079225.5:p.Thr1058Ala
XM_011532269.1:c.3244A>G	XP_011530571.1:p.Thr1082Ala
XM_011532269.3:c.3244A>G	XP_011530571.1:p.Thr1082Ala
XM_024454225.1:c.2950A>G	XP_024309993.1:p.Thr984Ala
NM_024949.6:c.3172A>G MANE Select	NP_079225.5:p.Thr1058Ala