Canonical Allele Identifier: CA10636213

Gene: WDR72

Linked Data

• ClinVar Variation Id: 316509
• ClinVar RCV Id: RCV000365012
• dbSNP Id: rs201133545
• gnomAD v2: 15-53807205-C-CATATATAT
• gnomAD v3: 15-53515008-C-CATATATAT
• gnomAD v4: 15-53515008-C-CATATATAT
• MyVariant Identifiers: chr15:g.53807206_53807213dupATATATAT (hg19) ; chr15:g.53807207_53807208insATATATAT (hg19) ; chr15:g.53807205_53807206insATATATAT (hg19) ; chr15:g.53515009_53515016dupATATATAT (hg38) ; chr15:g.53515010_53515011insATATATAT (hg38) ; chr15:g.53515008_53515009insATATATAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.53515018_53515025dup , CM000677.2:g.53515018_53515025dup	GRCh38
NC_000015.9:g.53807215_53807222dup , CM000677.1:g.53807215_53807222dup	GRCh37
NC_000015.8:g.51594507_51594514dup	NCBI36
NG_017034.2:g.249647_249654dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360509.10:c.*2683_*2690dup MANE Select	ENSP00000353699.5:n.*2683_*2690dup
ENST00000396328.5:c.*2683_*2690dup	ENSP00000379619.1:n.*2683_*2690dup
ENST00000567224.1:n.3058_3065dup
ENST00000614174.4:c.2950_2957dup	ENSP00000477754.1:n.2950_2957dup
NM_001277176.1:c.*2683_*2690dup	NP_001264105.1:n.*2683_*2690dup
NM_182758.3:c.*2683_*2690dup	NP_877435.3:n.*2683_*2690dup
NR_102334.1:n.6232_6239dup
NR_102335.1:n.3058_3065dup
NR_102336.1:n.3035_3042dup
XM_011521433.1:c.*2683_*2690dup	XP_011519735.1:n.*2683_*2690dup
XM_011521434.1:c.*2683_*2690dup	XP_011519736.1:n.*2683_*2690dup
XM_011521435.1:c.*2683_*2690dup	XP_011519737.1:n.*2683_*2690dup
XM_011521436.1:c.*2683_*2690dup	XP_011519738.1:n.*2683_*2690dup
XM_011521437.1:c.*2683_*2690dup	XP_011519739.1:n.*2683_*2690dup
XR_001751551.1:n.1410+115_1410+122dup
XR_001751552.1:n.1489+115_1489+122dup
XR_001751553.1:n.1502+115_1502+122dup
NM_182758.4:c.*2683_*2690dup MANE Select	NP_877435.3:n.*2683_*2690dup
NM_001277176.2:c.*2683_*2690dup	NP_001264105.1:n.*2683_*2690dup
NR_102334.2:n.6232_6239dup
NR_102335.2:n.3058_3065dup