Canonical Allele Identifier: CA7570885

Gene: WDR72

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.53615849A>C , CM000677.2:g.53615849A>C	GRCh38
NC_000015.9:g.53908046A>C , CM000677.1:g.53908046A>C	GRCh37
NC_000015.8:g.51695338A>C	NCBI36
NG_017034.2:g.148814T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_182758.4:c.2357T>G MANE Select	NP_877435.3:p.Val786Gly
ENST00000360509.10:c.2357T>G MANE Select	ENSP00000353699.5:p.Val786Gly
NM_182758.3:c.2357T>G	NP_877435.3:p.Val786Gly
NR_102334.1:n.2597T>G
NR_102334.2:n.2597T>G
ENST00000360509.9:c.2357T>G	ENSP00000353699.5:p.Val786Gly
ENST00000396328.5:c.2357T>G	ENSP00000379619.1:p.Val786Gly
ENST00000557913.5:c.2348T>G	ENSP00000453378.1:p.Val783Gly
ENST00000559418.5:c.2387T>G	ENSP00000452765.1:p.Val796Gly
XM_011521433.1:c.2357T>G	XP_011519735.1:p.Val786Gly
XM_011521433.2:c.2357T>G	XP_011519735.1:p.Val786Gly
XM_011521434.1:c.2357T>G	XP_011519736.1:p.Val786Gly
XM_011521435.1:c.2357T>G	XP_011519737.1:p.Val786Gly
XM_011521435.2:c.2357T>G	XP_011519737.1:p.Val786Gly
XM_011521436.1:c.2339T>G	XP_011519738.1:p.Val780Gly
XM_011521436.2:c.2339T>G	XP_011519738.1:p.Val780Gly
XM_011521437.1:c.2237T>G	XP_011519739.1:p.Val746Gly
XM_011521437.2:c.2237T>G	XP_011519739.1:p.Val746Gly
XM_017022061.1:c.2357T>G	XP_016877550.1:p.Val786Gly