Canonical Allele Identifier: CA2709721491

Gene: WDR36

Linked Data

• dbSNP Id: rs144429326

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111098316del , CM000667.2:g.111098316del	GRCh38
NC_000005.9:g.110434014del , CM000667.1:g.110434014del	GRCh37
NC_000005.8:g.110461913del	NCBI36
NG_008979.1:g.11145del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.292-406del MANE Select	ENSP00000424628.3:n.292-406del
ENST00000504122.2:n.174-406del
ENST00000505303.5:n.428-406del
ENST00000506538.6:c.460-406del	ENSP00000423067.2:n.460-406del
ENST00000513710.3:c.292-406del	ENSP00000424628.3:n.292-406del
ENST00000612402.4:c.460-406del	ENSP00000479950.1:n.460-406del
NM_139281.2:c.460-406del	NP_644810.1:n.460-406del
XM_011543163.1:c.460-406del	XP_011541465.1:n.460-406del
NM_139281.3:c.292-406del MANE Select	NP_644810.2:n.292-406del