Canonical Allele Identifier: CA358845785

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210588C>A (hg19) ; chr4:g.183289435C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289435C>A , CM000666.2:g.183289435C>A	GRCh38
NC_000004.11:g.184210588C>A , CM000666.1:g.184210588C>A	GRCh37
NC_000004.10:g.184447582C>A	NCBI36
NG_051586.1:g.195801C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3184C>A MANE Select	ENSP00000384222.3:p.Pro1062Thr
ENST00000403733.7:c.3184C>A	ENSP00000384222.3:p.Pro1062Thr
ENST00000427431.5:c.*2576C>A	ENSP00000393342.1:n.*2576C>A
ENST00000438543.5:c.*980C>A	ENSP00000413521.1:n.*980C>A
ENST00000448232.6:c.3256C>A	ENSP00000398577.2:p.Pro1086Thr
ENST00000504005.5:c.2230C>A	ENSP00000427569.1:p.Pro744Thr
ENST00000508747.1:c.568C>A	ENSP00000420835.1:p.Pro190Thr
ENST00000513834.5:c.3037C>A	ENSP00000425054.1:p.Pro1013Thr
NM_024949.5:c.3184C>A	NP_079225.5:p.Pro1062Thr
XM_011532269.1:c.3256C>A	XP_011530571.1:p.Pro1086Thr
XM_011532269.3:c.3256C>A	XP_011530571.1:p.Pro1086Thr
XM_024454225.1:c.2962C>A	XP_024309993.1:p.Pro988Thr
NM_024949.6:c.3184C>A MANE Select	NP_079225.5:p.Pro1062Thr