Canonical Allele Identifier: CA2504575343

Gene: WDR36

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111098547_111098548insGGAAAGGGGGAT , CM000667.2:g.111098547_111098548insGGAAAGGGGGAT	GRCh38
NC_000005.9:g.110434245_110434246insGGAAAGGGGGAT , CM000667.1:g.110434245_110434246insGGAAAGGGGGAT	GRCh37
NC_000005.8:g.110462144_110462145insGGAAAGGGGGAT	NCBI36
NG_008979.1:g.11376_11377insGGAAAGGGGGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.292-175_292-174insGGAAAGGGGGAT MANE Select	ENSP00000424628.3:n.292-175_292-174insGGAAAGGGGGAT
ENST00000504122.2:n.174-175_174-174insGGAAAGGGGGAT
ENST00000505303.5:n.428-175_428-174insGGAAAGGGGGAT
ENST00000506538.6:c.460-175_460-174insGGAAAGGGGGAT	ENSP00000423067.2:n.460-175_460-174insGGAAAGGGGGAT
ENST00000513710.3:c.292-175_292-174insGGAAAGGGGGAT	ENSP00000424628.3:n.292-175_292-174insGGAAAGGGGGAT
ENST00000612402.4:c.460-175_460-174insGGAAAGGGGGAT	ENSP00000479950.1:n.460-175_460-174insGGAAAGGGGGAT
NM_139281.2:c.460-175_460-174insGGAAAGGGGGAT	NP_644810.1:n.460-175_460-174insGGAAAGGGGGAT
XM_011543163.1:c.460-175_460-174insGGAAAGGGGGAT	XP_011541465.1:n.460-175_460-174insGGAAAGGGGGAT
NM_139281.3:c.292-175_292-174insGGAAAGGGGGAT MANE Select	NP_644810.2:n.292-175_292-174insGGAAAGGGGGAT