Canonical Allele Identifier: CA1572614345

Gene: WDR36

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111098441_111098444delinsGCCT , CM000667.2:g.111098441_111098444delinsGCCT	GRCh38
NC_000005.9:g.110434139_110434142delinsGCCT , CM000667.1:g.110434139_110434142delinsGCCT	GRCh37
NC_000005.8:g.110462038_110462041delinsGCCT	NCBI36
NG_008979.1:g.11270_11273delinsGCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.292-281_292-278delinsGCCT MANE Select	ENSP00000424628.3:n.292-281_292-278delinsGCCT
ENST00000504122.2:n.174-281_174-278delinsGCCT
ENST00000505303.5:n.428-281_428-278delinsGCCT
ENST00000506538.6:c.460-281_460-278delinsGCCT	ENSP00000423067.2:n.460-281_460-278delinsGCCT
ENST00000513710.3:c.292-281_292-278delinsGCCT	ENSP00000424628.3:n.292-281_292-278delinsGCCT
ENST00000612402.4:c.460-281_460-278delinsGCCT	ENSP00000479950.1:n.460-281_460-278delinsGCCT
NM_139281.2:c.460-281_460-278delinsGCCT	NP_644810.1:n.460-281_460-278delinsGCCT
XM_011543163.1:c.460-281_460-278delinsGCCT	XP_011541465.1:n.460-281_460-278delinsGCCT
NM_139281.3:c.292-281_292-278delinsGCCT MANE Select	NP_644810.2:n.292-281_292-278delinsGCCT