Canonical Allele Identifier: CA1572628273

Gene: WDR36

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111118944_111118946delinsAAT , CM000667.2:g.111118944_111118946delinsAAT	GRCh38
NC_000005.9:g.110454642_110454644delinsAAT , CM000667.1:g.110454642_110454644delinsAAT	GRCh37
NC_000005.8:g.110482541_110482543delinsAAT	NCBI36
NG_008979.1:g.31773_31775delinsAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.1797-69_1797-67delinsAAT MANE Select	ENSP00000424628.3:n.1797-69_1797-67delinsAAT
ENST00000506538.6:c.1965-69_1965-67delinsAAT	ENSP00000423067.2:n.1965-69_1965-67delinsAAT
ENST00000513710.3:c.1797-69_1797-67delinsAAT	ENSP00000424628.3:n.1797-69_1797-67delinsAAT
ENST00000612402.4:c.1965-69_1965-67delinsAAT	ENSP00000479950.1:n.1965-69_1965-67delinsAAT
NM_139281.2:c.1965-69_1965-67delinsAAT	NP_644810.1:n.1965-69_1965-67delinsAAT
XM_011543163.1:c.1965-69_1965-67delinsAAT	XP_011541465.1:n.1965-69_1965-67delinsAAT
NM_139281.3:c.1797-69_1797-67delinsAAT MANE Select	NP_644810.2:n.1797-69_1797-67delinsAAT