Canonical Allele Identifier: CA1572628188

Gene: WDR36

Linked Data

• dbSNP Id: rs1753506290

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111118748_111118749insAAA , CM000667.2:g.111118748_111118749insAAA	GRCh38
NC_000005.9:g.110454446_110454447insAAA , CM000667.1:g.110454446_110454447insAAA	GRCh37
NC_000005.8:g.110482345_110482346insAAA	NCBI36
NG_008979.1:g.31577_31578insAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.1797-265_1797-264insAAA MANE Select	ENSP00000424628.3:n.1797-265_1797-264insAAA
ENST00000506538.6:c.1965-265_1965-264insAAA	ENSP00000423067.2:n.1965-265_1965-264insAAA
ENST00000513710.3:c.1797-265_1797-264insAAA	ENSP00000424628.3:n.1797-265_1797-264insAAA
ENST00000612402.4:c.1965-265_1965-264insAAA	ENSP00000479950.1:n.1965-265_1965-264insAAA
NM_139281.2:c.1965-265_1965-264insAAA	NP_644810.1:n.1965-265_1965-264insAAA
XM_011543163.1:c.1965-265_1965-264insAAA	XP_011541465.1:n.1965-265_1965-264insAAA
NM_139281.3:c.1797-265_1797-264insAAA MANE Select	NP_644810.2:n.1797-265_1797-264insAAA