Canonical Allele Identifier: CA2243000588

Gene: WDR81

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1728624_1728626delinsTTG , CM000679.2:g.1728624_1728626delinsTTG	GRCh38
NC_000017.10:g.1631918_1631920delinsTTG , CM000679.1:g.1631918_1631920delinsTTG	GRCh37
NC_000017.9:g.1578668_1578670delinsTTG	NCBI36
NG_032811.1:g.17102_17104delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409644.6:c.3665_3667delinsTTG MANE Select	ENSP00000386609.1:p.Leu1222=
ENST00000309182.9:c.512_514delinsTTG	ENSP00000312074.5:p.Leu171=
ENST00000409644.5:c.3665_3667delinsTTG	ENSP00000386609.1:p.Leu1222=
ENST00000418841.5:c.-88-3701_-88-3699delinsTTG	ENSP00000395198.1:n.-88-3701_-88-3699delinsTTG
ENST00000419248.5:c.-14-1756_-14-1754delinsTTG	ENSP00000407845.1:n.-14-1756_-14-1754delinsTTG
ENST00000437219.6:c.59-1756_59-1754delinsTTG	ENSP00000391074.2:n.59-1756_59-1754delinsTTG
ENST00000446363.5:c.-308-2131_-308-2129delinsTTG	ENSP00000401560.1:n.-308-2131_-308-2129delinsTTG
ENST00000455636.5:c.59-1756_59-1754delinsTTG	ENSP00000395226.1:n.59-1756_59-1754delinsTTG
ENST00000464528.5:n.1051_1053delinsTTG
ENST00000468539.5:c.63-3701_63-3699delinsTTG	ENSP00000460742.1:n.63-3701_63-3699delinsTTG
ENST00000492901.1:n.88-1756_88-1754delinsTTG
ENST00000575206.1:c.415_417delinsTTG
NM_001163673.1:c.59-1756_59-1754delinsTTG	NP_001157145.1:n.59-1756_59-1754delinsTTG
NM_001163809.1:c.3665_3667delinsTTG	NP_001157281.1:p.Leu1222=
NM_001163811.1:c.-14-1756_-14-1754delinsTTG	NP_001157283.1:n.-14-1756_-14-1754delinsTTG
NM_152348.3:c.512_514delinsTTG	NP_689561.2:p.Leu171=
XM_005256454.2:c.3665_3667delinsTTG	XP_005256511.1:p.Leu1222=
XM_011523650.1:c.3665_3667delinsTTG	XP_011521952.1:p.Leu1222=
XM_011523651.1:c.512_514delinsTTG	XP_011521953.1:p.Leu171=
XR_933973.1:n.3809_3811delinsTTG
XM_011523651.2:c.512_514delinsTTG	XP_011521953.1:p.Leu171=
XM_017024184.1:c.3665_3667delinsTTG	XP_016879673.1:p.Leu1222=
XR_001752427.1:n.3817_3819delinsTTG
XR_933973.2:n.3817_3819delinsTTG
NM_001163809.2:c.3665_3667delinsTTG MANE Select	NP_001157281.1:p.Leu1222=
NM_001163811.2:c.-14-1756_-14-1754delinsTTG	NP_001157283.1:n.-14-1756_-14-1754delinsTTG
NM_152348.4:c.512_514delinsTTG	NP_689561.2:p.Leu171=
NM_001163673.2:c.59-1756_59-1754delinsTTG	NP_001157145.1:n.59-1756_59-1754delinsTTG