Canonical Allele Identifier: CA8273536

Gene: WDR81

Linked Data

• ClinVar Variation Id: 734276
• ClinVar RCV Id: RCV000909674 ; RCV004551780
• dbSNP Id: rs200150228
• ExAC: 17:1635952 G / A
• gnomAD v2: 17-1635952-G-A
• gnomAD v3: 17-1732658-G-A
• gnomAD v4: 17-1732658-G-A
• MyVariant Identifiers: chr17:g.1635952G>A (hg19) ; chr17:g.1732658G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1732658G>A , CM000679.2:g.1732658G>A	GRCh38
NC_000017.10:g.1635952G>A , CM000679.1:g.1635952G>A	GRCh37
NC_000017.9:g.1582702G>A	NCBI36
NG_032811.1:g.21136G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409644.6:c.4324-8G>A MANE Select	ENSP00000386609.1:n.4324-8G>A
ENST00000309182.9:c.1171-8G>A	ENSP00000312074.5:n.1171-8G>A
ENST00000409644.5:c.4324-8G>A	ENSP00000386609.1:n.4324-8G>A
ENST00000418841.5:c.79-8G>A	ENSP00000395198.1:n.79-8G>A
ENST00000419248.5:c.643-8G>A	ENSP00000407845.1:n.643-8G>A
ENST00000437219.6:c.715-8G>A	ENSP00000391074.2:n.715-8G>A
ENST00000446363.5:c.241-8G>A	ENSP00000401560.1:n.241-8G>A
ENST00000464528.5:n.1710-8G>A
ENST00000468539.5:c.229-8G>A	ENSP00000460742.1:n.229-8G>A
ENST00000474958.2:c.385-8G>A
ENST00000495411.1:n.242-8G>A
NM_001163673.1:c.715-8G>A	NP_001157145.1:n.715-8G>A
NM_001163809.1:c.4324-8G>A	NP_001157281.1:n.4324-8G>A
NM_001163811.1:c.643-8G>A	NP_001157283.1:n.643-8G>A
NM_152348.3:c.1171-8G>A	NP_689561.2:n.1171-8G>A
XM_005256454.2:c.4324-8G>A	XP_005256511.1:n.4324-8G>A
XM_011523650.1:c.4324-8G>A	XP_011521952.1:n.4324-8G>A
XM_011523651.1:c.1171-8G>A	XP_011521953.1:n.1171-8G>A
XR_933973.1:n.4468-8G>A
XM_011523651.2:c.1171-8G>A	XP_011521953.1:n.1171-8G>A
XM_017024184.1:c.4324-8G>A	XP_016879673.1:n.4324-8G>A
XR_001752427.1:n.4476-8G>A
XR_933973.2:n.4476-8G>A
NM_001163809.2:c.4324-8G>A MANE Select	NP_001157281.1:n.4324-8G>A
NM_001163811.2:c.643-8G>A	NP_001157283.1:n.643-8G>A
NM_152348.4:c.1171-8G>A	NP_689561.2:n.1171-8G>A
NM_001163673.2:c.715-8G>A	NP_001157145.1:n.715-8G>A