Canonical Allele Identifier: CA1071760585
Gene: WWC2 HGNC NCBI

Linked Data

dbSNP Id: rs1738350057

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.183289139_183289140del , CM000666.2:g.183289139_183289140del GRCh38
NC_000004.11:g.184210292_184210293del , CM000666.1:g.184210292_184210293del GRCh37
NC_000004.10:g.184447286_184447287del NCBI36
NG_051586.1:g.195505_195506del

Transcript Alleles

HGVS Amino-acid Change
ENST00000403733.8:c.3142-254_3142-253del MANE Select ENSP00000384222.3:n.3142-254_3142-253del
ENST00000403733.7:c.3142-254_3142-253del ENSP00000384222.3:n.3142-254_3142-253del
ENST00000427431.5:c.*2534-254_*2534-253del ENSP00000393342.1:n.*2534-254_*2534-253del
ENST00000438543.5:c.*938-254_*938-253del ENSP00000413521.1:n.*938-254_*938-253del
ENST00000448232.6:c.3214-254_3214-253del ENSP00000398577.2:n.3214-254_3214-253del
ENST00000504005.5:c.2188-254_2188-253del ENSP00000427569.1:n.2188-254_2188-253del
ENST00000508747.1:c.526-254_526-253del ENSP00000420835.1:n.526-254_526-253del
ENST00000513834.5:c.2995-254_2995-253del ENSP00000425054.1:n.2995-254_2995-253del
NM_024949.5:c.3142-254_3142-253del NP_079225.5:n.3142-254_3142-253del
XM_011532269.1:c.3214-254_3214-253del XP_011530571.1:n.3214-254_3214-253del
XM_011532269.3:c.3214-254_3214-253del XP_011530571.1:n.3214-254_3214-253del
XM_024454225.1:c.2920-254_2920-253del XP_024309993.1:n.2920-254_2920-253del
NM_024949.6:c.3142-254_3142-253del MANE Select NP_079225.5:n.3142-254_3142-253del