Canonical Allele Identifier: CA10636252

Gene: WDR72

Linked Data

• ClinVar Variation Id: 316547
• ClinVar RCV Id: RCV000299679
• dbSNP Id: rs72745124
• gnomAD v2: 15-53808162-A-G
• gnomAD v3: 15-53515965-A-G
• gnomAD v4: 15-53515965-A-G
• MyVariant Identifiers: chr15:g.53808162A>G (hg19) ; chr15:g.53515965A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.53515965A>G , CM000677.2:g.53515965A>G	GRCh38
NC_000015.9:g.53808162A>G , CM000677.1:g.53808162A>G	GRCh37
NC_000015.8:g.51595454A>G	NCBI36
NG_017034.2:g.248698T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360509.10:c.*1734T>C MANE Select	ENSP00000353699.5:n.*1734T>C
ENST00000360509.9:c.*1734T>C	ENSP00000353699.5:n.*1734T>C
ENST00000396328.5:c.*1734T>C	ENSP00000379619.1:n.*1734T>C
ENST00000557913.5:c.*1734T>C	ENSP00000453378.1:n.*1734T>C
ENST00000567224.1:n.2109T>C
ENST00000614174.4:c.2001T>C	ENSP00000477754.1:n.2001T>C
NM_001277176.1:c.*1734T>C	NP_001264105.1:n.*1734T>C
NM_182758.3:c.*1734T>C	NP_877435.3:n.*1734T>C
NR_102334.1:n.5283T>C
NR_102335.1:n.2109T>C
NR_102336.1:n.2086T>C
XM_011521433.1:c.*1734T>C	XP_011519735.1:n.*1734T>C
XM_011521434.1:c.*1734T>C	XP_011519736.1:n.*1734T>C
XM_011521435.1:c.*1734T>C	XP_011519737.1:n.*1734T>C
XM_011521436.1:c.*1734T>C	XP_011519738.1:n.*1734T>C
XM_011521437.1:c.*1734T>C	XP_011519739.1:n.*1734T>C
XM_011521433.2:c.*1734T>C	XP_011519735.1:n.*1734T>C
XM_011521435.2:c.*1734T>C	XP_011519737.1:n.*1734T>C
XM_017022061.1:c.*1734T>C	XP_016877550.1:n.*1734T>C
XR_001751551.1:n.1410+1062A>G
XR_001751552.1:n.1489+1062A>G
XR_001751553.1:n.1502+1062A>G
NM_182758.4:c.*1734T>C MANE Select	NP_877435.3:n.*1734T>C
NM_001277176.2:c.*1734T>C	NP_001264105.1:n.*1734T>C
NR_102334.2:n.5283T>C
NR_102335.2:n.2109T>C