Canonical Allele Identifier: CA358846253
Gene: WWC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.183289550T>G , CM000666.2:g.183289550T>G GRCh38
NC_000004.11:g.184210703T>G , CM000666.1:g.184210703T>G GRCh37
NC_000004.10:g.184447697T>G NCBI36
NG_051586.1:g.195916T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000403733.8:c.3299T>G MANE Select ENSP00000384222.3:p.Leu1100Arg
ENST00000403733.7:c.3299T>G ENSP00000384222.3:p.Leu1100Arg
ENST00000427431.5:c.*2691T>G ENSP00000393342.1:n.*2691T>G
ENST00000438543.5:c.*1095T>G ENSP00000413521.1:n.*1095T>G
ENST00000448232.6:c.3371T>G ENSP00000398577.2:p.Leu1124Arg
ENST00000504005.5:c.2345T>G ENSP00000427569.1:p.Leu782Arg
ENST00000508747.1:c.683T>G ENSP00000420835.1:p.Leu228Arg
ENST00000513834.5:c.3152T>G ENSP00000425054.1:p.Leu1051Arg
NM_024949.5:c.3299T>G NP_079225.5:p.Leu1100Arg
XM_011532269.1:c.3371T>G XP_011530571.1:p.Leu1124Arg
XM_011532269.3:c.3371T>G XP_011530571.1:p.Leu1124Arg
XM_024454225.1:c.3077T>G XP_024309993.1:p.Leu1026Arg
NM_024949.6:c.3299T>G MANE Select NP_079225.5:p.Leu1100Arg