Canonical Allele Identifier: CA1572614135

Gene: WDR36

Linked Data

• dbSNP Id: rs1753034693

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111098188_111098192del , CM000667.2:g.111098188_111098192del	GRCh38
NC_000005.9:g.110433886_110433890del , CM000667.1:g.110433886_110433890del	GRCh37
NC_000005.8:g.110461785_110461789del	NCBI36
NG_008979.1:g.11017_11021del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.292-534_292-530del MANE Select	ENSP00000424628.3:n.292-534_292-530del
ENST00000504122.2:n.174-534_174-530del
ENST00000505303.5:n.428-534_428-530del
ENST00000506538.6:c.460-534_460-530del	ENSP00000423067.2:n.460-534_460-530del
ENST00000513710.3:c.292-534_292-530del	ENSP00000424628.3:n.292-534_292-530del
ENST00000612402.4:c.460-534_460-530del	ENSP00000479950.1:n.460-534_460-530del
NM_139281.2:c.460-534_460-530del	NP_644810.1:n.460-534_460-530del
XM_011543163.1:c.460-534_460-530del	XP_011541465.1:n.460-534_460-530del
NM_139281.3:c.292-534_292-530del MANE Select	NP_644810.2:n.292-534_292-530del