Canonical Allele Identifier: CA358846397
Gene: WWC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.183289618A>T , CM000666.2:g.183289618A>T GRCh38
NC_000004.11:g.184210771A>T , CM000666.1:g.184210771A>T GRCh37
NC_000004.10:g.184447765A>T NCBI36
NG_051586.1:g.195984A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000403733.8:c.3367A>T MANE Select ENSP00000384222.3:p.Lys1123Ter
ENST00000403733.7:c.3367A>T ENSP00000384222.3:p.Lys1123Ter
ENST00000427431.5:c.*2759A>T ENSP00000393342.1:n.*2759A>T
ENST00000438543.5:c.*1163A>T ENSP00000413521.1:n.*1163A>T
ENST00000448232.6:c.3439A>T ENSP00000398577.2:p.Lys1147Ter
ENST00000504005.5:c.2413A>T ENSP00000427569.1:p.Lys805Ter
ENST00000508747.1:c.751A>T ENSP00000420835.1:p.Lys251Ter
ENST00000513834.5:c.3220A>T ENSP00000425054.1:p.Lys1074Ter
NM_024949.5:c.3367A>T NP_079225.5:p.Lys1123Ter
XM_011532269.1:c.3439A>T XP_011530571.1:p.Lys1147Ter
XM_011532269.3:c.3439A>T XP_011530571.1:p.Lys1147Ter
XM_024454225.1:c.3145A>T XP_024309993.1:p.Lys1049Ter
NM_024949.6:c.3367A>T MANE Select NP_079225.5:p.Lys1123Ter