Canonical Allele Identifier: CA2767910308

Gene: WDR36

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111118974_111118975insCAA , CM000667.2:g.111118974_111118975insCAA	GRCh38
NC_000005.9:g.110454672_110454673insCAA , CM000667.1:g.110454672_110454673insCAA	GRCh37
NC_000005.8:g.110482571_110482572insCAA	NCBI36
NG_008979.1:g.31803_31804insCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.1797-39_1797-38insCAA MANE Select	ENSP00000424628.3:n.1797-39_1797-38insCAA
ENST00000506538.6:c.1965-39_1965-38insCAA	ENSP00000423067.2:n.1965-39_1965-38insCAA
ENST00000513710.3:c.1797-39_1797-38insCAA	ENSP00000424628.3:n.1797-39_1797-38insCAA
ENST00000612402.4:c.1965-39_1965-38insCAA	ENSP00000479950.1:n.1965-39_1965-38insCAA
NM_139281.2:c.1965-39_1965-38insCAA	NP_644810.1:n.1965-39_1965-38insCAA
XM_011543163.1:c.1965-39_1965-38insCAA	XP_011541465.1:n.1965-39_1965-38insCAA
NM_139281.3:c.1797-39_1797-38insCAA MANE Select	NP_644810.2:n.1797-39_1797-38insCAA