Canonical Allele Identifier: CA1572614221

Gene: WDR36

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111098297_111098298delinsAC , CM000667.2:g.111098297_111098298delinsAC	GRCh38
NC_000005.9:g.110433995_110433996delinsAC , CM000667.1:g.110433995_110433996delinsAC	GRCh37
NC_000005.8:g.110461894_110461895delinsAC	NCBI36
NG_008979.1:g.11126_11127delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.292-425_292-424delinsAC MANE Select	ENSP00000424628.3:n.292-425_292-424delinsAC
ENST00000504122.2:n.174-425_174-424delinsAC
ENST00000505303.5:n.428-425_428-424delinsAC
ENST00000506538.6:c.460-425_460-424delinsAC	ENSP00000423067.2:n.460-425_460-424delinsAC
ENST00000513710.3:c.292-425_292-424delinsAC	ENSP00000424628.3:n.292-425_292-424delinsAC
ENST00000612402.4:c.460-425_460-424delinsAC	ENSP00000479950.1:n.460-425_460-424delinsAC
NM_139281.2:c.460-425_460-424delinsAC	NP_644810.1:n.460-425_460-424delinsAC
XM_011543163.1:c.460-425_460-424delinsAC	XP_011541465.1:n.460-425_460-424delinsAC
NM_139281.3:c.292-425_292-424delinsAC MANE Select	NP_644810.2:n.292-425_292-424delinsAC