Canonical Allele Identifier: CA1572614128

Gene: WDR36

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111098186_111098188delinsCAG , CM000667.2:g.111098186_111098188delinsCAG	GRCh38
NC_000005.9:g.110433884_110433886delinsCAG , CM000667.1:g.110433884_110433886delinsCAG	GRCh37
NC_000005.8:g.110461783_110461785delinsCAG	NCBI36
NG_008979.1:g.11015_11017delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.292-536_292-534delinsCAG MANE Select	ENSP00000424628.3:n.292-536_292-534delinsCAG
ENST00000504122.2:n.174-536_174-534delinsCAG
ENST00000505303.5:n.428-536_428-534delinsCAG
ENST00000506538.6:c.460-536_460-534delinsCAG	ENSP00000423067.2:n.460-536_460-534delinsCAG
ENST00000513710.3:c.292-536_292-534delinsCAG	ENSP00000424628.3:n.292-536_292-534delinsCAG
ENST00000612402.4:c.460-536_460-534delinsCAG	ENSP00000479950.1:n.460-536_460-534delinsCAG
NM_139281.2:c.460-536_460-534delinsCAG	NP_644810.1:n.460-536_460-534delinsCAG
XM_011543163.1:c.460-536_460-534delinsCAG	XP_011541465.1:n.460-536_460-534delinsCAG
NM_139281.3:c.292-536_292-534delinsCAG MANE Select	NP_644810.2:n.292-536_292-534delinsCAG