Canonical Allele Identifier: CA2243000016

Gene: WDR81

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1728337_1728340delinsCGAG , CM000679.2:g.1728337_1728340delinsCGAG	GRCh38
NC_000017.10:g.1631631_1631634delinsCGAG , CM000679.1:g.1631631_1631634delinsCGAG	GRCh37
NC_000017.9:g.1578381_1578384delinsCGAG	NCBI36
NG_032811.1:g.16815_16818delinsCGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409644.6:c.3378_3381delinsCGAG MANE Select	ENSP00000386609.1:p.Asp1126=
ENST00000309182.9:c.225_228delinsCGAG	ENSP00000312074.5:p.Asp75=
ENST00000409644.5:c.3378_3381delinsCGAG	ENSP00000386609.1:p.Asp1126=
ENST00000418841.5:c.-89+3551_-89+3554delinsCGAG	ENSP00000395198.1:n.-89+3551_-89+3554delinsCGAG
ENST00000419248.5:c.-14-2043_-14-2040delinsCGAG	ENSP00000407845.1:n.-14-2043_-14-2040delinsCGAG
ENST00000437219.6:c.59-2043_59-2040delinsCGAG	ENSP00000391074.2:n.59-2043_59-2040delinsCGAG
ENST00000446363.5:c.-308-2418_-308-2415delinsCGAG	ENSP00000401560.1:n.-308-2418_-308-2415delinsCGAG
ENST00000455636.5:c.59-2043_59-2040delinsCGAG	ENSP00000395226.1:n.59-2043_59-2040delinsCGAG
ENST00000464528.5:n.764_767delinsCGAG
ENST00000468539.5:c.63-3988_63-3985delinsCGAG	ENSP00000460742.1:n.63-3988_63-3985delinsCGAG
ENST00000492901.1:n.88-2043_88-2040delinsCGAG
ENST00000575206.1:c.128_131delinsCGAG
NM_001163673.1:c.59-2043_59-2040delinsCGAG	NP_001157145.1:n.59-2043_59-2040delinsCGAG
NM_001163809.1:c.3378_3381delinsCGAG	NP_001157281.1:p.Asp1126=
NM_001163811.1:c.-14-2043_-14-2040delinsCGAG	NP_001157283.1:n.-14-2043_-14-2040delinsCGAG
NM_152348.3:c.225_228delinsCGAG	NP_689561.2:p.Asp75=
XM_005256454.2:c.3378_3381delinsCGAG	XP_005256511.1:p.Asp1126=
XM_011523650.1:c.3378_3381delinsCGAG	XP_011521952.1:p.Asp1126=
XM_011523651.1:c.225_228delinsCGAG	XP_011521953.1:p.Asp75=
XR_933973.1:n.3522_3525delinsCGAG
XM_011523651.2:c.225_228delinsCGAG	XP_011521953.1:p.Asp75=
XM_017024184.1:c.3378_3381delinsCGAG	XP_016879673.1:p.Asp1126=
XR_001752427.1:n.3530_3533delinsCGAG
XR_933973.2:n.3530_3533delinsCGAG
NM_001163809.2:c.3378_3381delinsCGAG MANE Select	NP_001157281.1:p.Asp1126=
NM_001163811.2:c.-14-2043_-14-2040delinsCGAG	NP_001157283.1:n.-14-2043_-14-2040delinsCGAG
NM_152348.4:c.225_228delinsCGAG	NP_689561.2:p.Asp75=
NM_001163673.2:c.59-2043_59-2040delinsCGAG	NP_001157145.1:n.59-2043_59-2040delinsCGAG