Canonical Allele Identifier: CA2635265778

Gene: WDR81

Linked Data

• gnomAD v4: 17-1728736-C-CTTG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1728736_1728737insTTG , CM000679.2:g.1728736_1728737insTTG	GRCh38
NC_000017.10:g.1632030_1632031insTTG , CM000679.1:g.1632030_1632031insTTG	GRCh37
NC_000017.9:g.1578780_1578781insTTG	NCBI36
NG_032811.1:g.17214_17215insTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409644.6:c.3667+110_3667+111insTTG MANE Select	ENSP00000386609.1:n.3667+110_3667+111insTTG
ENST00000309182.9:c.514+110_514+111insTTG	ENSP00000312074.5:n.514+110_514+111insTTG
ENST00000409644.5:c.3667+110_3667+111insTTG	ENSP00000386609.1:n.3667+110_3667+111insTTG
ENST00000418841.5:c.-88-3589_-88-3588insTTG	ENSP00000395198.1:n.-88-3589_-88-3588insTTG
ENST00000419248.5:c.-14-1644_-14-1643insTTG	ENSP00000407845.1:n.-14-1644_-14-1643insTTG
ENST00000437219.6:c.59-1644_59-1643insTTG	ENSP00000391074.2:n.59-1644_59-1643insTTG
ENST00000446363.5:c.-308-2019_-308-2018insTTG	ENSP00000401560.1:n.-308-2019_-308-2018insTTG
ENST00000455636.5:c.59-1644_59-1643insTTG	ENSP00000395226.1:n.59-1644_59-1643insTTG
ENST00000464528.5:n.1053+110_1053+111insTTG
ENST00000468539.5:c.63-3589_63-3588insTTG	ENSP00000460742.1:n.63-3589_63-3588insTTG
ENST00000492901.1:n.88-1644_88-1643insTTG
ENST00000575206.1:c.417+110_417+111insTTG
NM_001163673.1:c.59-1644_59-1643insTTG	NP_001157145.1:n.59-1644_59-1643insTTG
NM_001163809.1:c.3667+110_3667+111insTTG	NP_001157281.1:n.3667+110_3667+111insTTG
NM_001163811.1:c.-14-1644_-14-1643insTTG	NP_001157283.1:n.-14-1644_-14-1643insTTG
NM_152348.3:c.514+110_514+111insTTG	NP_689561.2:n.514+110_514+111insTTG
XM_005256454.2:c.3667+110_3667+111insTTG	XP_005256511.1:n.3667+110_3667+111insTTG
XM_011523650.1:c.3667+110_3667+111insTTG	XP_011521952.1:n.3667+110_3667+111insTTG
XM_011523651.1:c.514+110_514+111insTTG	XP_011521953.1:n.514+110_514+111insTTG
XR_933973.1:n.3811+110_3811+111insTTG
XM_011523651.2:c.514+110_514+111insTTG	XP_011521953.1:n.514+110_514+111insTTG
XM_017024184.1:c.3667+110_3667+111insTTG	XP_016879673.1:n.3667+110_3667+111insTTG
XR_001752427.1:n.3819+110_3819+111insTTG
XR_933973.2:n.3819+110_3819+111insTTG
NM_001163809.2:c.3667+110_3667+111insTTG MANE Select	NP_001157281.1:n.3667+110_3667+111insTTG
NM_001163811.2:c.-14-1644_-14-1643insTTG	NP_001157283.1:n.-14-1644_-14-1643insTTG
NM_152348.4:c.514+110_514+111insTTG	NP_689561.2:n.514+110_514+111insTTG
NM_001163673.2:c.59-1644_59-1643insTTG	NP_001157145.1:n.59-1644_59-1643insTTG