Canonical Allele Identifier: CA111773944

Gene: WWC2

Linked Data

• dbSNP Id: rs376418534
• MyVariant Identifiers: chr4:g.184210943_184210949del (hg19) ; chr4:g.183289790_183289796del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289797_183289803del , CM000666.2:g.183289797_183289803del	GRCh38
NC_000004.11:g.184210950_184210956del , CM000666.1:g.184210950_184210956del	GRCh37
NC_000004.10:g.184447944_184447950del	NCBI36
NG_051586.1:g.196163_196169del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3384+162_3384+168del MANE Select	ENSP00000384222.3:n.3384+162_3384+168del
ENST00000403733.7:c.3384+162_3384+168del	ENSP00000384222.3:n.3384+162_3384+168del
ENST00000427431.5:c.*2776+162_*2776+168del	ENSP00000393342.1:n.*2776+162_*2776+168del
ENST00000438543.5:c.*1180+162_*1180+168del	ENSP00000413521.1:n.*1180+162_*1180+168del
ENST00000448232.6:c.3456+162_3456+168del	ENSP00000398577.2:n.3456+162_3456+168del
ENST00000504005.5:c.2430+162_2430+168del	ENSP00000427569.1:n.2430+162_2430+168del
ENST00000508747.1:c.768+162_768+168del	ENSP00000420835.1:n.768+162_768+168del
ENST00000513834.5:c.3237+162_3237+168del	ENSP00000425054.1:n.3237+162_3237+168del
NM_024949.5:c.3384+162_3384+168del	NP_079225.5:n.3384+162_3384+168del
XM_011532269.1:c.3456+162_3456+168del	XP_011530571.1:n.3456+162_3456+168del
XM_011532269.3:c.3456+162_3456+168del	XP_011530571.1:n.3456+162_3456+168del
XM_024454225.1:c.3162+162_3162+168del	XP_024309993.1:n.3162+162_3162+168del
NM_024949.6:c.3384+162_3384+168del MANE Select	NP_079225.5:n.3384+162_3384+168del