Canonical Allele Identifier: CA557393611

Gene: WWC2

Linked Data

• gnomAD v2: 4-184210942-C-CTT
• gnomAD v3: 4-183289789-C-CTT
• gnomAD v4: 4-183289789-C-CTT
• MyVariant Identifiers: chr4:g.184210946_184210947insTT (hg19) ; chr4:g.183289793_183289794insTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289802_183289803dup , CM000666.2:g.183289802_183289803dup	GRCh38
NC_000004.11:g.184210955_184210956dup , CM000666.1:g.184210955_184210956dup	GRCh37
NC_000004.10:g.184447949_184447950dup	NCBI36
NG_051586.1:g.196168_196169dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3384+167_3384+168dup MANE Select	ENSP00000384222.3:n.3384+167_3384+168dup
ENST00000403733.7:c.3384+167_3384+168dup	ENSP00000384222.3:n.3384+167_3384+168dup
ENST00000427431.5:c.*2776+167_*2776+168dup	ENSP00000393342.1:n.*2776+167_*2776+168dup
ENST00000438543.5:c.*1180+167_*1180+168dup	ENSP00000413521.1:n.*1180+167_*1180+168dup
ENST00000448232.6:c.3456+167_3456+168dup	ENSP00000398577.2:n.3456+167_3456+168dup
ENST00000504005.5:c.2430+167_2430+168dup	ENSP00000427569.1:n.2430+167_2430+168dup
ENST00000508747.1:c.768+167_768+168dup	ENSP00000420835.1:n.768+167_768+168dup
ENST00000513834.5:c.3237+167_3237+168dup	ENSP00000425054.1:n.3237+167_3237+168dup
NM_024949.5:c.3384+167_3384+168dup	NP_079225.5:n.3384+167_3384+168dup
XM_011532269.1:c.3456+167_3456+168dup	XP_011530571.1:n.3456+167_3456+168dup
XM_011532269.3:c.3456+167_3456+168dup	XP_011530571.1:n.3456+167_3456+168dup
XM_024454225.1:c.3162+167_3162+168dup	XP_024309993.1:n.3162+167_3162+168dup
NM_024949.6:c.3384+167_3384+168dup MANE Select	NP_079225.5:n.3384+167_3384+168dup