Canonical Allele Identifier: CA1071760822

Gene: WWC2

Linked Data

• dbSNP Id: rs1738382033
• gnomAD v3: 4-183289803-TCCAA-T
• gnomAD v4: 4-183289803-TCCAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289804_183289807del , CM000666.2:g.183289804_183289807del	GRCh38
NC_000004.11:g.184210957_184210960del , CM000666.1:g.184210957_184210960del	GRCh37
NC_000004.10:g.184447951_184447954del	NCBI36
NG_051586.1:g.196170_196173del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3384+169_3384+172del MANE Select	ENSP00000384222.3:n.3384+169_3384+172del
ENST00000403733.7:c.3384+169_3384+172del	ENSP00000384222.3:n.3384+169_3384+172del
ENST00000427431.5:c.*2776+169_*2776+172del	ENSP00000393342.1:n.*2776+169_*2776+172del
ENST00000438543.5:c.*1180+169_*1180+172del	ENSP00000413521.1:n.*1180+169_*1180+172del
ENST00000448232.6:c.3456+169_3456+172del	ENSP00000398577.2:n.3456+169_3456+172del
ENST00000504005.5:c.2430+169_2430+172del	ENSP00000427569.1:n.2430+169_2430+172del
ENST00000508747.1:c.768+169_768+172del	ENSP00000420835.1:n.768+169_768+172del
ENST00000513834.5:c.3237+169_3237+172del	ENSP00000425054.1:n.3237+169_3237+172del
NM_024949.5:c.3384+169_3384+172del	NP_079225.5:n.3384+169_3384+172del
XM_011532269.1:c.3456+169_3456+172del	XP_011530571.1:n.3456+169_3456+172del
XM_011532269.3:c.3456+169_3456+172del	XP_011530571.1:n.3456+169_3456+172del
XM_024454225.1:c.3162+169_3162+172del	XP_024309993.1:n.3162+169_3162+172del
NM_024949.6:c.3384+169_3384+172del MANE Select	NP_079225.5:n.3384+169_3384+172del