Canonical Allele Identifier: CA2243000491

Gene: WDR81

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1728538_1728541delinsTGTG , CM000679.2:g.1728538_1728541delinsTGTG	GRCh38
NC_000017.10:g.1631832_1631835delinsTGTG , CM000679.1:g.1631832_1631835delinsTGTG	GRCh37
NC_000017.9:g.1578582_1578585delinsTGTG	NCBI36
NG_032811.1:g.17016_17019delinsTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409644.6:c.3579_3582delinsTGTG MANE Select	ENSP00000386609.1:p.Val1193=
ENST00000309182.9:c.426_429delinsTGTG	ENSP00000312074.5:p.Val142=
ENST00000409644.5:c.3579_3582delinsTGTG	ENSP00000386609.1:p.Val1193=
ENST00000418841.5:c.-89+3752_-89+3755delinsTGTG	ENSP00000395198.1:n.-89+3752_-89+3755delinsTGTG
ENST00000419248.5:c.-14-1842_-14-1839delinsTGTG	ENSP00000407845.1:n.-14-1842_-14-1839delinsTGTG
ENST00000437219.6:c.59-1842_59-1839delinsTGTG	ENSP00000391074.2:n.59-1842_59-1839delinsTGTG
ENST00000446363.5:c.-308-2217_-308-2214delinsTGTG	ENSP00000401560.1:n.-308-2217_-308-2214delinsTGTG
ENST00000455636.5:c.59-1842_59-1839delinsTGTG	ENSP00000395226.1:n.59-1842_59-1839delinsTGTG
ENST00000464528.5:n.965_968delinsTGTG
ENST00000468539.5:c.63-3787_63-3784delinsTGTG	ENSP00000460742.1:n.63-3787_63-3784delinsTGTG
ENST00000492901.1:n.88-1842_88-1839delinsTGTG
ENST00000575206.1:c.329_332delinsTGTG
NM_001163673.1:c.59-1842_59-1839delinsTGTG	NP_001157145.1:n.59-1842_59-1839delinsTGTG
NM_001163809.1:c.3579_3582delinsTGTG	NP_001157281.1:p.Val1193=
NM_001163811.1:c.-14-1842_-14-1839delinsTGTG	NP_001157283.1:n.-14-1842_-14-1839delinsTGTG
NM_152348.3:c.426_429delinsTGTG	NP_689561.2:p.Val142=
XM_005256454.2:c.3579_3582delinsTGTG	XP_005256511.1:p.Val1193=
XM_011523650.1:c.3579_3582delinsTGTG	XP_011521952.1:p.Val1193=
XM_011523651.1:c.426_429delinsTGTG	XP_011521953.1:p.Val142=
XR_933973.1:n.3723_3726delinsTGTG
XM_011523651.2:c.426_429delinsTGTG	XP_011521953.1:p.Val142=
XM_017024184.1:c.3579_3582delinsTGTG	XP_016879673.1:p.Val1193=
XR_001752427.1:n.3731_3734delinsTGTG
XR_933973.2:n.3731_3734delinsTGTG
NM_001163809.2:c.3579_3582delinsTGTG MANE Select	NP_001157281.1:p.Val1193=
NM_001163811.2:c.-14-1842_-14-1839delinsTGTG	NP_001157283.1:n.-14-1842_-14-1839delinsTGTG
NM_152348.4:c.426_429delinsTGTG	NP_689561.2:p.Val142=
NM_001163673.2:c.59-1842_59-1839delinsTGTG	NP_001157145.1:n.59-1842_59-1839delinsTGTG