Canonical Allele Identifier: CA1572628213

Gene: WDR36

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111118812_111118816delinsTTAAG , CM000667.2:g.111118812_111118816delinsTTAAG	GRCh38
NC_000005.9:g.110454510_110454514delinsTTAAG , CM000667.1:g.110454510_110454514delinsTTAAG	GRCh37
NC_000005.8:g.110482409_110482413delinsTTAAG	NCBI36
NG_008979.1:g.31641_31645delinsTTAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.1797-201_1797-197delinsTTAAG MANE Select	ENSP00000424628.3:n.1797-201_1797-197delinsTTAAG
ENST00000506538.6:c.1965-201_1965-197delinsTTAAG	ENSP00000423067.2:n.1965-201_1965-197delinsTTAAG
ENST00000513710.3:c.1797-201_1797-197delinsTTAAG	ENSP00000424628.3:n.1797-201_1797-197delinsTTAAG
ENST00000612402.4:c.1965-201_1965-197delinsTTAAG	ENSP00000479950.1:n.1965-201_1965-197delinsTTAAG
NM_139281.2:c.1965-201_1965-197delinsTTAAG	NP_644810.1:n.1965-201_1965-197delinsTTAAG
XM_011543163.1:c.1965-201_1965-197delinsTTAAG	XP_011541465.1:n.1965-201_1965-197delinsTTAAG
NM_139281.3:c.1797-201_1797-197delinsTTAAG MANE Select	NP_644810.2:n.1797-201_1797-197delinsTTAAG