Canonical Allele Identifier: CA124902596

Gene: WDR36

Linked Data

• dbSNP Id: rs35075896

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111098199dup , CM000667.2:g.111098199dup	GRCh38
NC_000005.9:g.110433897dup , CM000667.1:g.110433897dup	GRCh37
NC_000005.8:g.110461796dup	NCBI36
NG_008979.1:g.11028dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.292-523dup MANE Select	ENSP00000424628.3:n.292-523dup
ENST00000504122.2:n.174-523dup
ENST00000505303.5:n.428-523dup
ENST00000506538.6:c.460-523dup	ENSP00000423067.2:n.460-523dup
ENST00000513710.3:c.292-523dup	ENSP00000424628.3:n.292-523dup
ENST00000612402.4:c.460-523dup	ENSP00000479950.1:n.460-523dup
NM_139281.2:c.460-523dup	NP_644810.1:n.460-523dup
XM_011543163.1:c.460-523dup	XP_011541465.1:n.460-523dup
NM_139281.3:c.292-523dup MANE Select	NP_644810.2:n.292-523dup