Canonical Allele Identifier: CA645584795

Gene: WDR81

Linked Data

• COSMIC: COSM111487

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1728221_1728227del , CM000679.2:g.1728221_1728227del	GRCh38
NC_000017.10:g.1631515_1631521del , CM000679.1:g.1631515_1631521del	GRCh37
NC_000017.9:g.1578265_1578271del	NCBI36
NG_032811.1:g.16699_16705del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409644.6:c.3262_3268del MANE Select	ENSP00000386609.1:p.Gly1088MetfsTer2
ENST00000309182.9:c.109_115del	ENSP00000312074.5:p.Gly37MetfsTer2
ENST00000409644.5:c.3262_3268del	ENSP00000386609.1:p.Gly1088MetfsTer2
ENST00000418841.5:c.-89+3435_-89+3441del	ENSP00000395198.1:n.-89+3435_-89+3441del
ENST00000419248.5:c.-14-2159_-14-2153del	ENSP00000407845.1:n.-14-2159_-14-2153del
ENST00000437219.6:c.59-2159_59-2153del	ENSP00000391074.2:n.59-2159_59-2153del
ENST00000446363.5:c.-308-2534_-308-2528del	ENSP00000401560.1:n.-308-2534_-308-2528del
ENST00000455636.5:c.59-2159_59-2153del	ENSP00000395226.1:n.59-2159_59-2153del
ENST00000464528.5:n.648_654del
ENST00000468539.5:c.63-4104_63-4098del	ENSP00000460742.1:n.63-4104_63-4098del
ENST00000492901.1:n.88-2159_88-2153del
ENST00000575206.1:c.12_18del
NM_001163673.1:c.59-2159_59-2153del	NP_001157145.1:n.59-2159_59-2153del
NM_001163809.1:c.3262_3268del	NP_001157281.1:p.Gly1088MetfsTer2
NM_001163811.1:c.-14-2159_-14-2153del	NP_001157283.1:n.-14-2159_-14-2153del
NM_152348.3:c.109_115del	NP_689561.2:p.Gly37MetfsTer2
XM_005256454.2:c.3262_3268del	XP_005256511.1:p.Gly1088MetfsTer2
XM_011523650.1:c.3262_3268del	XP_011521952.1:p.Gly1088MetfsTer2
XM_011523651.1:c.109_115del	XP_011521953.1:p.Gly37MetfsTer2
XR_933973.1:n.3406_3412del
XM_011523651.2:c.109_115del	XP_011521953.1:p.Gly37MetfsTer2
XM_017024184.1:c.3262_3268del	XP_016879673.1:p.Gly1088MetfsTer2
XR_001752427.1:n.3414_3420del
XR_933973.2:n.3414_3420del
NM_001163809.2:c.3262_3268del MANE Select	NP_001157281.1:p.Gly1088MetfsTer2
NM_001163811.2:c.-14-2159_-14-2153del	NP_001157283.1:n.-14-2159_-14-2153del
NM_152348.4:c.109_115del	NP_689561.2:p.Gly37MetfsTer2
NM_001163673.2:c.59-2159_59-2153del	NP_001157145.1:n.59-2159_59-2153del