Canonical Allele Identifier: CA111773973

Gene: WWC2

Linked Data

• dbSNP Id: rs141079671
• gnomAD v2: 4-184210963-CAA-C
• gnomAD v3: 4-183289810-CAA-C
• gnomAD v4: 4-183289810-CAA-C
• MyVariant Identifiers: chr4:g.184210964_184210965del (hg19) ; chr4:g.183289811_183289812del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289814_183289815del , CM000666.2:g.183289814_183289815del	GRCh38
NC_000004.11:g.184210967_184210968del , CM000666.1:g.184210967_184210968del	GRCh37
NC_000004.10:g.184447961_184447962del	NCBI36
NG_051586.1:g.196180_196181del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3384+179_3384+180del MANE Select	ENSP00000384222.3:n.3384+179_3384+180del
ENST00000403733.7:c.3384+179_3384+180del	ENSP00000384222.3:n.3384+179_3384+180del
ENST00000427431.5:c.*2776+179_*2776+180del	ENSP00000393342.1:n.*2776+179_*2776+180del
ENST00000438543.5:c.*1180+179_*1180+180del	ENSP00000413521.1:n.*1180+179_*1180+180del
ENST00000448232.6:c.3456+179_3456+180del	ENSP00000398577.2:n.3456+179_3456+180del
ENST00000504005.5:c.2430+179_2430+180del	ENSP00000427569.1:n.2430+179_2430+180del
ENST00000508747.1:c.768+179_768+180del	ENSP00000420835.1:n.768+179_768+180del
ENST00000513834.5:c.3237+179_3237+180del	ENSP00000425054.1:n.3237+179_3237+180del
NM_024949.5:c.3384+179_3384+180del	NP_079225.5:n.3384+179_3384+180del
XM_011532269.1:c.3456+179_3456+180del	XP_011530571.1:n.3456+179_3456+180del
XM_011532269.3:c.3456+179_3456+180del	XP_011530571.1:n.3456+179_3456+180del
XM_024454225.1:c.3162+179_3162+180del	XP_024309993.1:n.3162+179_3162+180del
NM_024949.6:c.3384+179_3384+180del MANE Select	NP_079225.5:n.3384+179_3384+180del