Canonical Allele Identifier: CA8273292

Gene: WDR81

Linked Data

• dbSNP Id: rs752609059
• ExAC: 17:1631865 AGAG / A
• gnomAD v2: 17-1631865-AGAG-A
• gnomAD v3: 17-1728571-AGAG-A
• gnomAD v4: 17-1728571-AGAG-A
• MyVariant Identifiers: chr17:g.1631866_1631868del (hg19) ; chr17:g.1728573_1728575del (hg38) ; chr17:g.1728572_1728574del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1728579_1728581del , CM000679.2:g.1728579_1728581del	GRCh38
NC_000017.10:g.1631873_1631875del , CM000679.1:g.1631873_1631875del	GRCh37
NC_000017.9:g.1578623_1578625del	NCBI36
NG_032811.1:g.17057_17059del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409644.6:c.3620_3622del MANE Select	ENSP00000386609.1:p.Glu1207del
ENST00000309182.9:c.467_469del	ENSP00000312074.5:p.Glu156del
ENST00000409644.5:c.3620_3622del	ENSP00000386609.1:p.Glu1207del
ENST00000418841.5:c.-88-3746_-88-3744del	ENSP00000395198.1:n.-88-3746_-88-3744del
ENST00000419248.5:c.-14-1801_-14-1799del	ENSP00000407845.1:n.-14-1801_-14-1799del
ENST00000437219.6:c.59-1801_59-1799del	ENSP00000391074.2:n.59-1801_59-1799del
ENST00000446363.5:c.-308-2176_-308-2174del	ENSP00000401560.1:n.-308-2176_-308-2174del
ENST00000455636.5:c.59-1801_59-1799del	ENSP00000395226.1:n.59-1801_59-1799del
ENST00000464528.5:n.1006_1008del
ENST00000468539.5:c.63-3746_63-3744del	ENSP00000460742.1:n.63-3746_63-3744del
ENST00000492901.1:n.88-1801_88-1799del
ENST00000575206.1:c.370_372del
NM_001163673.1:c.59-1801_59-1799del	NP_001157145.1:n.59-1801_59-1799del
NM_001163809.1:c.3620_3622del	NP_001157281.1:p.Glu1207del
NM_001163811.1:c.-14-1801_-14-1799del	NP_001157283.1:n.-14-1801_-14-1799del
NM_152348.3:c.467_469del	NP_689561.2:p.Glu156del
XM_005256454.2:c.3620_3622del	XP_005256511.1:p.Glu1207del
XM_011523650.1:c.3620_3622del	XP_011521952.1:p.Glu1207del
XM_011523651.1:c.467_469del	XP_011521953.1:p.Glu156del
XR_933973.1:n.3764_3766del
XM_011523651.2:c.467_469del	XP_011521953.1:p.Glu156del
XM_017024184.1:c.3620_3622del	XP_016879673.1:p.Glu1207del
XR_001752427.1:n.3772_3774del
XR_933973.2:n.3772_3774del
NM_001163809.2:c.3620_3622del MANE Select	NP_001157281.1:p.Glu1207del
NM_001163811.2:c.-14-1801_-14-1799del	NP_001157283.1:n.-14-1801_-14-1799del
NM_152348.4:c.467_469del	NP_689561.2:p.Glu156del
NM_001163673.2:c.59-1801_59-1799del	NP_001157145.1:n.59-1801_59-1799del