Canonical Allele Identifier: CA2177890980

Gene: WDR72

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.53650793_53650798delinsCAACAA , CM000677.2:g.53650793_53650798delinsCAACAA	GRCh38
NC_000015.9:g.53942990_53942995delinsCAACAA , CM000677.1:g.53942990_53942995delinsCAACAA	GRCh37
NC_000015.8:g.51730282_51730287delinsCAACAA	NCBI36
NG_017034.2:g.113865_113870delinsTTGTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360509.10:c.1962+14774_1962+14779delinsTTGTTG MANE Select	ENSP00000353699.5:n.1962+14774_1962+14779delinsTTGTTG
ENST00000360509.9:c.1962+14774_1962+14779delinsTTGTTG	ENSP00000353699.5:n.1962+14774_1962+14779delinsTTGTTG
ENST00000396328.5:c.1962+14774_1962+14779delinsTTGTTG	ENSP00000379619.1:n.1962+14774_1962+14779delinsTTGTTG
ENST00000557913.5:c.1953+14774_1953+14779delinsTTGTTG	ENSP00000453378.1:n.1953+14774_1953+14779delinsTTGTTG
ENST00000559418.5:c.1992+14774_1992+14779delinsTTGTTG	ENSP00000452765.1:n.1992+14774_1992+14779delinsTTGTTG
ENST00000560036.1:c.1962+14774_1962+14779delinsTTGTTG	ENSP00000453813.1:n.1962+14774_1962+14779delinsTTGTTG
NM_182758.3:c.1962+14774_1962+14779delinsTTGTTG	NP_877435.3:n.1962+14774_1962+14779delinsTTGTTG
NR_102334.1:n.2202+14774_2202+14779delinsTTGTTG
XM_011521433.1:c.1962+14774_1962+14779delinsTTGTTG	XP_011519735.1:n.1962+14774_1962+14779delinsTTGTTG
XM_011521434.1:c.1962+14774_1962+14779delinsTTGTTG	XP_011519736.1:n.1962+14774_1962+14779delinsTTGTTG
XM_011521435.1:c.1962+14774_1962+14779delinsTTGTTG	XP_011519737.1:n.1962+14774_1962+14779delinsTTGTTG
XM_011521436.1:c.1944+14774_1944+14779delinsTTGTTG	XP_011519738.1:n.1944+14774_1944+14779delinsTTGTTG
XM_011521437.1:c.1842+14774_1842+14779delinsTTGTTG	XP_011519739.1:n.1842+14774_1842+14779delinsTTGTTG
XM_011521433.2:c.1962+14774_1962+14779delinsTTGTTG	XP_011519735.1:n.1962+14774_1962+14779delinsTTGTTG
XM_011521435.2:c.1962+14774_1962+14779delinsTTGTTG	XP_011519737.1:n.1962+14774_1962+14779delinsTTGTTG
XM_011521436.2:c.1944+14774_1944+14779delinsTTGTTG	XP_011519738.1:n.1944+14774_1944+14779delinsTTGTTG
XM_011521437.2:c.1842+14774_1842+14779delinsTTGTTG	XP_011519739.1:n.1842+14774_1842+14779delinsTTGTTG
XM_017022061.1:c.1962+14774_1962+14779delinsTTGTTG	XP_016877550.1:n.1962+14774_1962+14779delinsTTGTTG
NM_182758.4:c.1962+14774_1962+14779delinsTTGTTG MANE Select	NP_877435.3:n.1962+14774_1962+14779delinsTTGTTG
NR_102334.2:n.2202+14774_2202+14779delinsTTGTTG