Canonical Allele Identifier: CA2672776333

Gene: WWC2

Linked Data

• gnomAD v4: 4-183289503-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289504del , CM000666.2:g.183289504del	GRCh38
NC_000004.11:g.184210657del , CM000666.1:g.184210657del	GRCh37
NC_000004.10:g.184447651del	NCBI36
NG_051586.1:g.195870del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3253del MANE Select	ENSP00000384222.3:p.Asp1085MetfsTer6
ENST00000403733.7:c.3253del	ENSP00000384222.3:p.Asp1085MetfsTer6
ENST00000427431.5:c.*2645del	ENSP00000393342.1:n.*2645del
ENST00000438543.5:c.*1049del	ENSP00000413521.1:n.*1049del
ENST00000448232.6:c.3325del	ENSP00000398577.2:p.Asp1109MetfsTer6
ENST00000504005.5:c.2299del	ENSP00000427569.1:p.Asp767MetfsTer6
ENST00000508747.1:c.637del	ENSP00000420835.1:p.Asp213MetfsTer6
ENST00000513834.5:c.3106del	ENSP00000425054.1:p.Asp1036MetfsTer6
NM_024949.5:c.3253del	NP_079225.5:p.Asp1085MetfsTer6
XM_011532269.1:c.3325del	XP_011530571.1:p.Asp1109MetfsTer6
XM_011532269.3:c.3325del	XP_011530571.1:p.Asp1109MetfsTer6
XM_024454225.1:c.3031del	XP_024309993.1:p.Asp1011MetfsTer6
NM_024949.6:c.3253del MANE Select	NP_079225.5:p.Asp1085MetfsTer6