Canonical Allele Identifier: CA2243000775

Gene: WDR81

Linked Data

• dbSNP Id: rs1915479896
• gnomAD v4: 17-1728764-TAAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1728767_1728769del , CM000679.2:g.1728767_1728769del	GRCh38
NC_000017.10:g.1632061_1632063del , CM000679.1:g.1632061_1632063del	GRCh37
NC_000017.9:g.1578811_1578813del	NCBI36
NG_032811.1:g.17245_17247del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409644.6:c.3667+141_3667+143del MANE Select	ENSP00000386609.1:n.3667+141_3667+143del
ENST00000309182.9:c.514+141_514+143del	ENSP00000312074.5:n.514+141_514+143del
ENST00000409644.5:c.3667+141_3667+143del	ENSP00000386609.1:n.3667+141_3667+143del
ENST00000418841.5:c.-88-3558_-88-3556del	ENSP00000395198.1:n.-88-3558_-88-3556del
ENST00000419248.5:c.-14-1613_-14-1611del	ENSP00000407845.1:n.-14-1613_-14-1611del
ENST00000437219.6:c.59-1613_59-1611del	ENSP00000391074.2:n.59-1613_59-1611del
ENST00000446363.5:c.-308-1988_-308-1986del	ENSP00000401560.1:n.-308-1988_-308-1986del
ENST00000455636.5:c.59-1613_59-1611del	ENSP00000395226.1:n.59-1613_59-1611del
ENST00000464528.5:n.1053+141_1053+143del
ENST00000468539.5:c.63-3558_63-3556del	ENSP00000460742.1:n.63-3558_63-3556del
ENST00000492901.1:n.88-1613_88-1611del
ENST00000575206.1:c.417+141_417+143del
NM_001163673.1:c.59-1613_59-1611del	NP_001157145.1:n.59-1613_59-1611del
NM_001163809.1:c.3667+141_3667+143del	NP_001157281.1:n.3667+141_3667+143del
NM_001163811.1:c.-14-1613_-14-1611del	NP_001157283.1:n.-14-1613_-14-1611del
NM_152348.3:c.514+141_514+143del	NP_689561.2:n.514+141_514+143del
XM_005256454.2:c.3667+141_3667+143del	XP_005256511.1:n.3667+141_3667+143del
XM_011523650.1:c.3667+141_3667+143del	XP_011521952.1:n.3667+141_3667+143del
XM_011523651.1:c.514+141_514+143del	XP_011521953.1:n.514+141_514+143del
XR_933973.1:n.3811+141_3811+143del
XM_011523651.2:c.514+141_514+143del	XP_011521953.1:n.514+141_514+143del
XM_017024184.1:c.3667+141_3667+143del	XP_016879673.1:n.3667+141_3667+143del
XR_001752427.1:n.3819+141_3819+143del
XR_933973.2:n.3819+141_3819+143del
NM_001163809.2:c.3667+141_3667+143del MANE Select	NP_001157281.1:n.3667+141_3667+143del
NM_001163811.2:c.-14-1613_-14-1611del	NP_001157283.1:n.-14-1613_-14-1611del
NM_152348.4:c.514+141_514+143del	NP_689561.2:n.514+141_514+143del
NM_001163673.2:c.59-1613_59-1611del	NP_001157145.1:n.59-1613_59-1611del