Canonical Allele Identifier: CA392527202

Gene: WDR72

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.53613674A>C , CM000677.2:g.53613674A>C	GRCh38
NC_000015.9:g.53905871A>C , CM000677.1:g.53905871A>C	GRCh37
NC_000015.8:g.51693163A>C	NCBI36
NG_017034.2:g.150989T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_182758.4:c.2864T>G MANE Select	NP_877435.3:p.Leu955Ter
ENST00000360509.10:c.2864T>G MANE Select	ENSP00000353699.5:p.Leu955Ter
NM_182758.3:c.2864T>G	NP_877435.3:p.Leu955Ter
NR_102334.1:n.3104T>G
NR_102334.2:n.3104T>G
ENST00000360509.9:c.2864T>G	ENSP00000353699.5:p.Leu955Ter
ENST00000396328.5:c.2864T>G	ENSP00000379619.1:p.Leu955Ter
ENST00000557913.5:c.2855T>G	ENSP00000453378.1:p.Leu952Ter
ENST00000559418.5:c.2894T>G	ENSP00000452765.1:p.Leu965Ter
XM_011521433.1:c.2864T>G	XP_011519735.1:p.Leu955Ter
XM_011521433.2:c.2864T>G	XP_011519735.1:p.Leu955Ter
XM_011521434.1:c.2864T>G	XP_011519736.1:p.Leu955Ter
XM_011521435.1:c.2864T>G	XP_011519737.1:p.Leu955Ter
XM_011521435.2:c.2864T>G	XP_011519737.1:p.Leu955Ter
XM_011521436.1:c.2846T>G	XP_011519738.1:p.Leu949Ter
XM_011521436.2:c.2846T>G	XP_011519738.1:p.Leu949Ter
XM_011521437.1:c.2744T>G	XP_011519739.1:p.Leu915Ter
XM_011521437.2:c.2744T>G	XP_011519739.1:p.Leu915Ter
XM_017022061.1:c.2864T>G	XP_016877550.1:p.Leu955Ter