Canonical Allele Identifier: CA1139663993

Gene: WDR72

Linked Data

• ClinVar Variation Id: 886457
• ClinVar RCV Id: RCV001118663
• dbSNP Id: rs1891398511

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.53515229T>C , CM000677.2:g.53515229T>C	GRCh38
NC_000015.9:g.53807426T>C , CM000677.1:g.53807426T>C	GRCh37
NC_000015.8:g.51594718T>C	NCBI36
NG_017034.2:g.249434A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360509.10:c.*2470A>G MANE Select	ENSP00000353699.5:n.*2470A>G
ENST00000360509.9:c.*2470A>G	ENSP00000353699.5:n.*2470A>G
ENST00000396328.5:c.*2470A>G	ENSP00000379619.1:n.*2470A>G
ENST00000557913.5:c.*2470A>G	ENSP00000453378.1:n.*2470A>G
ENST00000567224.1:n.2845A>G
ENST00000614174.4:c.2737A>G	ENSP00000477754.1:n.2737A>G
NM_001277176.1:c.*2470A>G	NP_001264105.1:n.*2470A>G
NM_182758.3:c.*2470A>G	NP_877435.3:n.*2470A>G
NR_102334.1:n.6019A>G
NR_102335.1:n.2845A>G
NR_102336.1:n.2822A>G
XM_011521433.1:c.*2470A>G	XP_011519735.1:n.*2470A>G
XM_011521434.1:c.*2470A>G	XP_011519736.1:n.*2470A>G
XM_011521435.1:c.*2470A>G	XP_011519737.1:n.*2470A>G
XM_011521436.1:c.*2470A>G	XP_011519738.1:n.*2470A>G
XM_011521437.1:c.*2470A>G	XP_011519739.1:n.*2470A>G
XM_011521433.2:c.*2470A>G	XP_011519735.1:n.*2470A>G
XM_011521435.2:c.*2470A>G	XP_011519737.1:n.*2470A>G
XM_017022061.1:c.*2470A>G	XP_016877550.1:n.*2470A>G
XR_001751551.1:n.1410+326T>C
XR_001751552.1:n.1489+326T>C
XR_001751553.1:n.1502+326T>C
NM_182758.4:c.*2470A>G MANE Select	NP_877435.3:n.*2470A>G
NM_001277176.2:c.*2470A>G	NP_001264105.1:n.*2470A>G
NR_102334.2:n.6019A>G
NR_102335.2:n.2845A>G