Canonical Allele Identifier: CA397593462

Gene: WDR81

Linked Data

• gnomAD v4: 17-1728189-C-T
• MyVariant Identifiers: chr17:g.1631483C>T (hg19) ; chr17:g.1728189C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1728189C>T , CM000679.2:g.1728189C>T	GRCh38
NC_000017.10:g.1631483C>T , CM000679.1:g.1631483C>T	GRCh37
NC_000017.9:g.1578233C>T	NCBI36
NG_032811.1:g.16667C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409644.6:c.3230C>T MANE Select	ENSP00000386609.1:p.Ala1077Val
ENST00000309182.9:c.77C>T	ENSP00000312074.5:p.Ala26Val
ENST00000409644.5:c.3230C>T	ENSP00000386609.1:p.Ala1077Val
ENST00000418841.5:c.-89+3403C>T	ENSP00000395198.1:n.-89+3403C>T
ENST00000419248.5:c.-14-2191C>T	ENSP00000407845.1:n.-14-2191C>T
ENST00000437219.6:c.59-2191C>T	ENSP00000391074.2:n.59-2191C>T
ENST00000446363.5:c.-308-2566C>T	ENSP00000401560.1:n.-308-2566C>T
ENST00000455636.5:c.59-2191C>T	ENSP00000395226.1:n.59-2191C>T
ENST00000464528.5:n.616C>T
ENST00000468539.5:c.63-4136C>T	ENSP00000460742.1:n.63-4136C>T
ENST00000492901.1:n.88-2191C>T
NM_001163673.1:c.59-2191C>T	NP_001157145.1:n.59-2191C>T
NM_001163809.1:c.3230C>T	NP_001157281.1:p.Ala1077Val
NM_001163811.1:c.-14-2191C>T	NP_001157283.1:n.-14-2191C>T
NM_152348.3:c.77C>T	NP_689561.2:p.Ala26Val
XM_005256454.2:c.3230C>T	XP_005256511.1:p.Ala1077Val
XM_011523650.1:c.3230C>T	XP_011521952.1:p.Ala1077Val
XM_011523651.1:c.77C>T	XP_011521953.1:p.Ala26Val
XR_933973.1:n.3374C>T
XM_011523651.2:c.77C>T	XP_011521953.1:p.Ala26Val
XM_017024184.1:c.3230C>T	XP_016879673.1:p.Ala1077Val
XR_001752427.1:n.3382C>T
XR_933973.2:n.3382C>T
NM_001163809.2:c.3230C>T MANE Select	NP_001157281.1:p.Ala1077Val
NM_001163811.2:c.-14-2191C>T	NP_001157283.1:n.-14-2191C>T
NM_152348.4:c.77C>T	NP_689561.2:p.Ala26Val
NM_001163673.2:c.59-2191C>T	NP_001157145.1:n.59-2191C>T