Canonical Allele Identifier: CA497394442

Gene: WDR81

Linked Data

• MyVariant Identifiers: chr17:g.1631559T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1728265T>A , CM000679.2:g.1728265T>A	GRCh38
NC_000017.10:g.1631559T>A , CM000679.1:g.1631559T>A	GRCh37
NC_000017.9:g.1578309T>A	NCBI36
NG_032811.1:g.16743T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409644.6:c.3306T>A MANE Select	ENSP00000386609.1:p.Ala1102=
ENST00000309182.9:c.153T>A	ENSP00000312074.5:p.Ala51=
ENST00000409644.5:c.3306T>A	ENSP00000386609.1:p.Ala1102=
ENST00000418841.5:c.-89+3479T>A	ENSP00000395198.1:n.-89+3479T>A
ENST00000419248.5:c.-14-2115T>A	ENSP00000407845.1:n.-14-2115T>A
ENST00000437219.6:c.59-2115T>A	ENSP00000391074.2:n.59-2115T>A
ENST00000446363.5:c.-308-2490T>A	ENSP00000401560.1:n.-308-2490T>A
ENST00000455636.5:c.59-2115T>A	ENSP00000395226.1:n.59-2115T>A
ENST00000464528.5:n.692T>A
ENST00000468539.5:c.63-4060T>A	ENSP00000460742.1:n.63-4060T>A
ENST00000492901.1:n.88-2115T>A
ENST00000575206.1:c.56T>A
NM_001163673.1:c.59-2115T>A	NP_001157145.1:n.59-2115T>A
NM_001163809.1:c.3306T>A	NP_001157281.1:p.Ala1102=
NM_001163811.1:c.-14-2115T>A	NP_001157283.1:n.-14-2115T>A
NM_152348.3:c.153T>A	NP_689561.2:p.Ala51=
XM_005256454.2:c.3306T>A	XP_005256511.1:p.Ala1102=
XM_011523650.1:c.3306T>A	XP_011521952.1:p.Ala1102=
XM_011523651.1:c.153T>A	XP_011521953.1:p.Ala51=
XR_933973.1:n.3450T>A
XM_011523651.2:c.153T>A	XP_011521953.1:p.Ala51=
XM_017024184.1:c.3306T>A	XP_016879673.1:p.Ala1102=
XR_001752427.1:n.3458T>A
XR_933973.2:n.3458T>A
NM_001163809.2:c.3306T>A MANE Select	NP_001157281.1:p.Ala1102=
NM_001163811.2:c.-14-2115T>A	NP_001157283.1:n.-14-2115T>A
NM_152348.4:c.153T>A	NP_689561.2:p.Ala51=
NM_001163673.2:c.59-2115T>A	NP_001157145.1:n.59-2115T>A