Canonical Allele Identifier: CA7571542

Gene: WDR72

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.53733051C>A , CM000677.2:g.53733051C>A	GRCh38
NC_000015.9:g.54025248C>A , CM000677.1:g.54025248C>A	GRCh37
NC_000015.8:g.51812540C>A	NCBI36
NG_017034.2:g.31612G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_182758.4:c.99G>T MANE Select	NP_877435.3:p.Val33=
ENST00000360509.10:c.99G>T MANE Select	ENSP00000353699.5:p.Val33=
NM_182758.3:c.99G>T	NP_877435.3:p.Val33=
NR_102334.1:n.339G>T
NR_102334.2:n.339G>T
ENST00000360509.9:c.99G>T	ENSP00000353699.5:p.Val33=
ENST00000396328.5:c.99G>T	ENSP00000379619.1:p.Val33=
ENST00000557913.5:c.99G>T	ENSP00000453378.1:p.Val33=
ENST00000559418.5:c.99G>T	ENSP00000452765.1:p.Val33=
ENST00000560036.1:c.99G>T	ENSP00000453813.1:p.Val33=
XM_011521433.1:c.99G>T	XP_011519735.1:p.Val33=
XM_011521433.2:c.99G>T	XP_011519735.1:p.Val33=
XM_011521434.1:c.99G>T	XP_011519736.1:p.Val33=
XM_011521435.1:c.99G>T	XP_011519737.1:p.Val33=
XM_011521435.2:c.99G>T	XP_011519737.1:p.Val33=
XM_011521436.1:c.99G>T	XP_011519738.1:p.Val33=
XM_011521436.2:c.99G>T	XP_011519738.1:p.Val33=
XM_011521437.1:c.99G>T	XP_011519739.1:p.Val33=
XM_011521437.2:c.99G>T	XP_011519739.1:p.Val33=
XM_017022061.1:c.99G>T	XP_016877550.1:p.Val33=