Canonical Allele Identifier: CA1572628265

Gene: WDR36

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111118926_111118931delinsCCTTAT , CM000667.2:g.111118926_111118931delinsCCTTAT	GRCh38
NC_000005.9:g.110454624_110454629delinsCCTTAT , CM000667.1:g.110454624_110454629delinsCCTTAT	GRCh37
NC_000005.8:g.110482523_110482528delinsCCTTAT	NCBI36
NG_008979.1:g.31755_31760delinsCCTTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.1797-87_1797-82delinsCCTTAT MANE Select	ENSP00000424628.3:n.1797-87_1797-82delinsCCTTAT
ENST00000506538.6:c.1965-87_1965-82delinsCCTTAT	ENSP00000423067.2:n.1965-87_1965-82delinsCCTTAT
ENST00000513710.3:c.1797-87_1797-82delinsCCTTAT	ENSP00000424628.3:n.1797-87_1797-82delinsCCTTAT
ENST00000612402.4:c.1965-87_1965-82delinsCCTTAT	ENSP00000479950.1:n.1965-87_1965-82delinsCCTTAT
NM_139281.2:c.1965-87_1965-82delinsCCTTAT	NP_644810.1:n.1965-87_1965-82delinsCCTTAT
XM_011543163.1:c.1965-87_1965-82delinsCCTTAT	XP_011541465.1:n.1965-87_1965-82delinsCCTTAT
NM_139281.3:c.1797-87_1797-82delinsCCTTAT MANE Select	NP_644810.2:n.1797-87_1797-82delinsCCTTAT