Canonical Allele Identifier: CA561883918
Gene: WDR36 HGNC NCBI

Linked Data

dbSNP Id: rs1483556969

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111118959del , CM000667.2:g.111118959del GRCh38
NC_000005.9:g.110454657del , CM000667.1:g.110454657del GRCh37
NC_000005.8:g.110482556del NCBI36
NG_008979.1:g.31788del

Transcript Alleles

HGVS Amino-acid change
ENST00000513710.4:c.1797-54del MANE Select ENSP00000424628.3:n.1797-54del
ENST00000506538.6:c.1965-54del ENSP00000423067.2:n.1965-54del
ENST00000513710.3:c.1797-54del ENSP00000424628.3:n.1797-54del
ENST00000612402.4:c.1965-54del ENSP00000479950.1:n.1965-54del
NM_139281.2:c.1965-54del NP_644810.1:n.1965-54del
XM_011543163.1:c.1965-54del XP_011541465.1:n.1965-54del
NM_139281.3:c.1797-54del MANE Select NP_644810.2:n.1797-54del