Canonical Allele Identifier: CA557393615

Gene: WWC2

Linked Data

• gnomAD v2: 4-184210942-CTTTT-C
• gnomAD v3: 4-183289789-CTTTT-C
• gnomAD v4: 4-183289789-CTTTT-C
• MyVariant Identifiers: chr4:g.184210943_184210946del (hg19) ; chr4:g.183289790_183289793del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289800_183289803del , CM000666.2:g.183289800_183289803del	GRCh38
NC_000004.11:g.184210953_184210956del , CM000666.1:g.184210953_184210956del	GRCh37
NC_000004.10:g.184447947_184447950del	NCBI36
NG_051586.1:g.196166_196169del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3384+165_3384+168del MANE Select	ENSP00000384222.3:n.3384+165_3384+168del
ENST00000403733.7:c.3384+165_3384+168del	ENSP00000384222.3:n.3384+165_3384+168del
ENST00000427431.5:c.*2776+165_*2776+168del	ENSP00000393342.1:n.*2776+165_*2776+168del
ENST00000438543.5:c.*1180+165_*1180+168del	ENSP00000413521.1:n.*1180+165_*1180+168del
ENST00000448232.6:c.3456+165_3456+168del	ENSP00000398577.2:n.3456+165_3456+168del
ENST00000504005.5:c.2430+165_2430+168del	ENSP00000427569.1:n.2430+165_2430+168del
ENST00000508747.1:c.768+165_768+168del	ENSP00000420835.1:n.768+165_768+168del
ENST00000513834.5:c.3237+165_3237+168del	ENSP00000425054.1:n.3237+165_3237+168del
NM_024949.5:c.3384+165_3384+168del	NP_079225.5:n.3384+165_3384+168del
XM_011532269.1:c.3456+165_3456+168del	XP_011530571.1:n.3456+165_3456+168del
XM_011532269.3:c.3456+165_3456+168del	XP_011530571.1:n.3456+165_3456+168del
XM_024454225.1:c.3162+165_3162+168del	XP_024309993.1:n.3162+165_3162+168del
NM_024949.6:c.3384+165_3384+168del MANE Select	NP_079225.5:n.3384+165_3384+168del