Canonical Allele Identifier: CA1071760841

Gene: WWC2

Linked Data

• gnomAD v3: 4-183289809-C-CTTTTTT
• gnomAD v4: 4-183289809-C-CTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289809_183289810insTTTTTT , CM000666.2:g.183289809_183289810insTTTTTT	GRCh38
NC_000004.11:g.184210962_184210963insTTTTTT , CM000666.1:g.184210962_184210963insTTTTTT	GRCh37
NC_000004.10:g.184447956_184447957insTTTTTT	NCBI36
NG_051586.1:g.196175_196176insTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3384+174_3384+175insTTTTTT MANE Select	ENSP00000384222.3:n.3384+174_3384+175insTTTTTT
ENST00000403733.7:c.3384+174_3384+175insTTTTTT	ENSP00000384222.3:n.3384+174_3384+175insTTTTTT
ENST00000427431.5:c.*2776+174_*2776+175insTTTTTT	ENSP00000393342.1:n.*2776+174_*2776+175insTTTTTT
ENST00000438543.5:c.*1180+174_*1180+175insTTTTTT	ENSP00000413521.1:n.*1180+174_*1180+175insTTTTTT
ENST00000448232.6:c.3456+174_3456+175insTTTTTT	ENSP00000398577.2:n.3456+174_3456+175insTTTTTT
ENST00000504005.5:c.2430+174_2430+175insTTTTTT	ENSP00000427569.1:n.2430+174_2430+175insTTTTTT
ENST00000508747.1:c.768+174_768+175insTTTTTT	ENSP00000420835.1:n.768+174_768+175insTTTTTT
ENST00000513834.5:c.3237+174_3237+175insTTTTTT	ENSP00000425054.1:n.3237+174_3237+175insTTTTTT
NM_024949.5:c.3384+174_3384+175insTTTTTT	NP_079225.5:n.3384+174_3384+175insTTTTTT
XM_011532269.1:c.3456+174_3456+175insTTTTTT	XP_011530571.1:n.3456+174_3456+175insTTTTTT
XM_011532269.3:c.3456+174_3456+175insTTTTTT	XP_011530571.1:n.3456+174_3456+175insTTTTTT
XM_024454225.1:c.3162+174_3162+175insTTTTTT	XP_024309993.1:n.3162+174_3162+175insTTTTTT
NM_024949.6:c.3384+174_3384+175insTTTTTT MANE Select	NP_079225.5:n.3384+174_3384+175insTTTTTT