Canonical Allele Identifier: CA1572628316

Gene: WDR36

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111119014_111119016delinsCTT , CM000667.2:g.111119014_111119016delinsCTT	GRCh38
NC_000005.9:g.110454712_110454714delinsCTT , CM000667.1:g.110454712_110454714delinsCTT	GRCh37
NC_000005.8:g.110482611_110482613delinsCTT	NCBI36
NG_008979.1:g.31843_31845delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.1798_1800delinsCTT MANE Select	ENSP00000424628.3:p.Leu600=
ENST00000506538.6:c.1966_1968delinsCTT	ENSP00000423067.2:p.Leu656=
ENST00000513710.3:c.1798_1800delinsCTT	ENSP00000424628.3:p.Leu600=
ENST00000612402.4:c.1966_1968delinsCTT	ENSP00000479950.1:p.Leu656=
NM_139281.2:c.1966_1968delinsCTT	NP_644810.1:p.Leu656=
XM_011543163.1:c.1966_1968delinsCTT	XP_011541465.1:p.Leu656=
NM_139281.3:c.1798_1800delinsCTT MANE Select	NP_644810.2:p.Leu600=