Canonical Allele Identifier: CA1572628190

Gene: WDR36

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111118756_111118758delinsCCT , CM000667.2:g.111118756_111118758delinsCCT	GRCh38
NC_000005.9:g.110454454_110454456delinsCCT , CM000667.1:g.110454454_110454456delinsCCT	GRCh37
NC_000005.8:g.110482353_110482355delinsCCT	NCBI36
NG_008979.1:g.31585_31587delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.1797-257_1797-255delinsCCT MANE Select	ENSP00000424628.3:n.1797-257_1797-255delinsCCT
ENST00000506538.6:c.1965-257_1965-255delinsCCT	ENSP00000423067.2:n.1965-257_1965-255delinsCCT
ENST00000513710.3:c.1797-257_1797-255delinsCCT	ENSP00000424628.3:n.1797-257_1797-255delinsCCT
ENST00000612402.4:c.1965-257_1965-255delinsCCT	ENSP00000479950.1:n.1965-257_1965-255delinsCCT
NM_139281.2:c.1965-257_1965-255delinsCCT	NP_644810.1:n.1965-257_1965-255delinsCCT
XM_011543163.1:c.1965-257_1965-255delinsCCT	XP_011541465.1:n.1965-257_1965-255delinsCCT
NM_139281.3:c.1797-257_1797-255delinsCCT MANE Select	NP_644810.2:n.1797-257_1797-255delinsCCT