Canonical Allele Identifier: CA358845943
Gene: WWC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.183289474G>A , CM000666.2:g.183289474G>A GRCh38
NC_000004.11:g.184210627G>A , CM000666.1:g.184210627G>A GRCh37
NC_000004.10:g.184447621G>A NCBI36
NG_051586.1:g.195840G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000403733.8:c.3223G>A MANE Select ENSP00000384222.3:p.Ala1075Thr
ENST00000403733.7:c.3223G>A ENSP00000384222.3:p.Ala1075Thr
ENST00000427431.5:c.*2615G>A ENSP00000393342.1:n.*2615G>A
ENST00000438543.5:c.*1019G>A ENSP00000413521.1:n.*1019G>A
ENST00000448232.6:c.3295G>A ENSP00000398577.2:p.Ala1099Thr
ENST00000504005.5:c.2269G>A ENSP00000427569.1:p.Ala757Thr
ENST00000508747.1:c.607G>A ENSP00000420835.1:p.Ala203Thr
ENST00000513834.5:c.3076G>A ENSP00000425054.1:p.Ala1026Thr
NM_024949.5:c.3223G>A NP_079225.5:p.Ala1075Thr
XM_011532269.1:c.3295G>A XP_011530571.1:p.Ala1099Thr
XM_011532269.3:c.3295G>A XP_011530571.1:p.Ala1099Thr
XM_024454225.1:c.3001G>A XP_024309993.1:p.Ala1001Thr
NM_024949.6:c.3223G>A MANE Select NP_079225.5:p.Ala1075Thr