Canonical Allele Identifier: CA2578377229

Gene: WDR36

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111119100_111119101del , CM000667.2:g.111119100_111119101del	GRCh38
NC_000005.9:g.110454798_110454799del , CM000667.1:g.110454798_110454799del	GRCh37
NC_000005.8:g.110482697_110482698del	NCBI36
NG_008979.1:g.31929_31930del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.1884_1885del MANE Select	ENSP00000424628.3:p.Asp628GlufsTer?
ENST00000506538.6:c.2052_2053del	ENSP00000423067.2:p.Asp684GlufsTer?
ENST00000513710.3:c.1884_1885del	ENSP00000424628.3:p.Asp628GlufsTer?
ENST00000612402.4:c.2052_2053del	ENSP00000479950.1:p.Asp684GlufsTer?
NM_139281.2:c.2052_2053del	NP_644810.1:p.Asp684GlufsTer?
XM_011543163.1:c.2052_2053del	XP_011541465.1:p.Asp684GlufsTer?
NM_139281.3:c.1884_1885del MANE Select	NP_644810.2:p.Asp628GlufsTer?