Canonical Allele Identifier: CA7570824

Gene: WDR72

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.53615520G>A , CM000677.2:g.53615520G>A	GRCh38
NC_000015.9:g.53907717G>A , CM000677.1:g.53907717G>A	GRCh37
NC_000015.8:g.51695009G>A	NCBI36
NG_017034.2:g.149143C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_182758.4:c.2686C>T MANE Select	NP_877435.3:p.Arg896Ter
ENST00000360509.10:c.2686C>T MANE Select	ENSP00000353699.5:p.Arg896Ter
NM_182758.3:c.2686C>T	NP_877435.3:p.Arg896Ter
NR_102334.1:n.2926C>T
NR_102334.2:n.2926C>T
ENST00000360509.9:c.2686C>T	ENSP00000353699.5:p.Arg896Ter
ENST00000396328.5:c.2686C>T	ENSP00000379619.1:p.Arg896Ter
ENST00000557913.5:c.2677C>T	ENSP00000453378.1:p.Arg893Ter
ENST00000559418.5:c.2716C>T	ENSP00000452765.1:p.Arg906Ter
XM_011521433.1:c.2686C>T	XP_011519735.1:p.Arg896Ter
XM_011521433.2:c.2686C>T	XP_011519735.1:p.Arg896Ter
XM_011521434.1:c.2686C>T	XP_011519736.1:p.Arg896Ter
XM_011521435.1:c.2686C>T	XP_011519737.1:p.Arg896Ter
XM_011521435.2:c.2686C>T	XP_011519737.1:p.Arg896Ter
XM_011521436.1:c.2668C>T	XP_011519738.1:p.Arg890Ter
XM_011521436.2:c.2668C>T	XP_011519738.1:p.Arg890Ter
XM_011521437.1:c.2566C>T	XP_011519739.1:p.Arg856Ter
XM_011521437.2:c.2566C>T	XP_011519739.1:p.Arg856Ter
XM_017022061.1:c.2686C>T	XP_016877550.1:p.Arg896Ter