Canonical Allele Identifier: CA2840981583

Gene: WDR36

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111119206_111119207insAAA , CM000667.2:g.111119206_111119207insAAA	GRCh38
NC_000005.9:g.110454904_110454905insAAA , CM000667.1:g.110454904_110454905insAAA	GRCh37
NC_000005.8:g.110482803_110482804insAAA	NCBI36
NG_008979.1:g.32035_32036insAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513710.4:c.1904+86_1904+87insAAA MANE Select	ENSP00000424628.3:n.1904+86_1904+87insAAA
ENST00000506538.6:c.2072+86_2072+87insAAA	ENSP00000423067.2:n.2072+86_2072+87insAAA
ENST00000513710.3:c.1904+86_1904+87insAAA	ENSP00000424628.3:n.1904+86_1904+87insAAA
ENST00000612402.4:c.2072+86_2072+87insAAA	ENSP00000479950.1:n.2072+86_2072+87insAAA
NM_139281.2:c.2072+86_2072+87insAAA	NP_644810.1:n.2072+86_2072+87insAAA
XM_011543163.1:c.2072+86_2072+87insAAA	XP_011541465.1:n.2072+86_2072+87insAAA
NM_139281.3:c.1904+86_1904+87insAAA MANE Select	NP_644810.2:n.1904+86_1904+87insAAA