Canonical Allele Identifier: CA1572628208

Gene: WDR36

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111118797_111118800delinsATGT , CM000667.2:g.111118797_111118800delinsATGT	GRCh38
NC_000005.9:g.110454495_110454498delinsATGT , CM000667.1:g.110454495_110454498delinsATGT	GRCh37
NC_000005.8:g.110482394_110482397delinsATGT	NCBI36
NG_008979.1:g.31626_31629delinsATGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.1797-216_1797-213delinsATGT MANE Select	ENSP00000424628.3:n.1797-216_1797-213delinsATGT
ENST00000506538.6:c.1965-216_1965-213delinsATGT	ENSP00000423067.2:n.1965-216_1965-213delinsATGT
ENST00000513710.3:c.1797-216_1797-213delinsATGT	ENSP00000424628.3:n.1797-216_1797-213delinsATGT
ENST00000612402.4:c.1965-216_1965-213delinsATGT	ENSP00000479950.1:n.1965-216_1965-213delinsATGT
NM_139281.2:c.1965-216_1965-213delinsATGT	NP_644810.1:n.1965-216_1965-213delinsATGT
XM_011543163.1:c.1965-216_1965-213delinsATGT	XP_011541465.1:n.1965-216_1965-213delinsATGT
NM_139281.3:c.1797-216_1797-213delinsATGT MANE Select	NP_644810.2:n.1797-216_1797-213delinsATGT