Canonical Allele Identifier: CA397593849

Gene: WDR81

Linked Data

• dbSNP Id: rs1369707743
• gnomAD v2: 17-1631636-G-T
• gnomAD v4: 17-1728342-G-T
• MyVariant Identifiers: chr17:g.1631636G>T (hg19) ; chr17:g.1728342G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1728342G>T , CM000679.2:g.1728342G>T	GRCh38
NC_000017.10:g.1631636G>T , CM000679.1:g.1631636G>T	GRCh37
NC_000017.9:g.1578386G>T	NCBI36
NG_032811.1:g.16820G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409644.6:c.3383G>T MANE Select	ENSP00000386609.1:p.Gly1128Val
ENST00000309182.9:c.230G>T	ENSP00000312074.5:p.Gly77Val
ENST00000409644.5:c.3383G>T	ENSP00000386609.1:p.Gly1128Val
ENST00000418841.5:c.-89+3556G>T	ENSP00000395198.1:n.-89+3556G>T
ENST00000419248.5:c.-14-2038G>T	ENSP00000407845.1:n.-14-2038G>T
ENST00000437219.6:c.59-2038G>T	ENSP00000391074.2:n.59-2038G>T
ENST00000446363.5:c.-308-2413G>T	ENSP00000401560.1:n.-308-2413G>T
ENST00000455636.5:c.59-2038G>T	ENSP00000395226.1:n.59-2038G>T
ENST00000464528.5:n.769G>T
ENST00000468539.5:c.63-3983G>T	ENSP00000460742.1:n.63-3983G>T
ENST00000492901.1:n.88-2038G>T
ENST00000575206.1:c.133G>T
NM_001163673.1:c.59-2038G>T	NP_001157145.1:n.59-2038G>T
NM_001163809.1:c.3383G>T	NP_001157281.1:p.Gly1128Val
NM_001163811.1:c.-14-2038G>T	NP_001157283.1:n.-14-2038G>T
NM_152348.3:c.230G>T	NP_689561.2:p.Gly77Val
XM_005256454.2:c.3383G>T	XP_005256511.1:p.Gly1128Val
XM_011523650.1:c.3383G>T	XP_011521952.1:p.Gly1128Val
XM_011523651.1:c.230G>T	XP_011521953.1:p.Gly77Val
XR_933973.1:n.3527G>T
XM_011523651.2:c.230G>T	XP_011521953.1:p.Gly77Val
XM_017024184.1:c.3383G>T	XP_016879673.1:p.Gly1128Val
XR_001752427.1:n.3535G>T
XR_933973.2:n.3535G>T
NM_001163809.2:c.3383G>T MANE Select	NP_001157281.1:p.Gly1128Val
NM_001163811.2:c.-14-2038G>T	NP_001157283.1:n.-14-2038G>T
NM_152348.4:c.230G>T	NP_689561.2:p.Gly77Val
NM_001163673.2:c.59-2038G>T	NP_001157145.1:n.59-2038G>T