Canonical Allele Identifier: CA1071760828

Gene: WWC2

Linked Data

• gnomAD v3: 4-183289807-A-ATTTT
• gnomAD v4: 4-183289807-A-ATTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289807_183289808insTTTT , CM000666.2:g.183289807_183289808insTTTT	GRCh38
NC_000004.11:g.184210960_184210961insTTTT , CM000666.1:g.184210960_184210961insTTTT	GRCh37
NC_000004.10:g.184447954_184447955insTTTT	NCBI36
NG_051586.1:g.196173_196174insTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3384+172_3384+173insTTTT MANE Select	ENSP00000384222.3:n.3384+172_3384+173insTTTT
ENST00000403733.7:c.3384+172_3384+173insTTTT	ENSP00000384222.3:n.3384+172_3384+173insTTTT
ENST00000427431.5:c.*2776+172_*2776+173insTTTT	ENSP00000393342.1:n.*2776+172_*2776+173insTTTT
ENST00000438543.5:c.*1180+172_*1180+173insTTTT	ENSP00000413521.1:n.*1180+172_*1180+173insTTTT
ENST00000448232.6:c.3456+172_3456+173insTTTT	ENSP00000398577.2:n.3456+172_3456+173insTTTT
ENST00000504005.5:c.2430+172_2430+173insTTTT	ENSP00000427569.1:n.2430+172_2430+173insTTTT
ENST00000508747.1:c.768+172_768+173insTTTT	ENSP00000420835.1:n.768+172_768+173insTTTT
ENST00000513834.5:c.3237+172_3237+173insTTTT	ENSP00000425054.1:n.3237+172_3237+173insTTTT
NM_024949.5:c.3384+172_3384+173insTTTT	NP_079225.5:n.3384+172_3384+173insTTTT
XM_011532269.1:c.3456+172_3456+173insTTTT	XP_011530571.1:n.3456+172_3456+173insTTTT
XM_011532269.3:c.3456+172_3456+173insTTTT	XP_011530571.1:n.3456+172_3456+173insTTTT
XM_024454225.1:c.3162+172_3162+173insTTTT	XP_024309993.1:n.3162+172_3162+173insTTTT
NM_024949.6:c.3384+172_3384+173insTTTT MANE Select	NP_079225.5:n.3384+172_3384+173insTTTT