Canonical Allele Identifier: CA1572628341

Gene: WDR36

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111119065_111119079delinsCCTACTGGAGACTTT , CM000667.2:g.111119065_111119079delinsCCTACTGGAGACTTT	GRCh38
NC_000005.9:g.110454763_110454777delinsCCTACTGGAGACTTT , CM000667.1:g.110454763_110454777delinsCCTACTGGAGACTTT	GRCh37
NC_000005.8:g.110482662_110482676delinsCCTACTGGAGACTTT	NCBI36
NG_008979.1:g.31894_31908delinsCCTACTGGAGACTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.1849_1863delinsCCTACTGGAGACTTT MANE Select	ENSP00000424628.3:p.Pro617=
ENST00000506538.6:c.2017_2031delinsCCTACTGGAGACTTT	ENSP00000423067.2:p.Pro673=
ENST00000513710.3:c.1849_1863delinsCCTACTGGAGACTTT	ENSP00000424628.3:p.Pro617=
ENST00000612402.4:c.2017_2031delinsCCTACTGGAGACTTT	ENSP00000479950.1:p.Pro673=
NM_139281.2:c.2017_2031delinsCCTACTGGAGACTTT	NP_644810.1:p.Pro673=
XM_011543163.1:c.2017_2031delinsCCTACTGGAGACTTT	XP_011541465.1:p.Pro673=
NM_139281.3:c.1849_1863delinsCCTACTGGAGACTTT MANE Select	NP_644810.2:p.Pro617=