Canonical Allele Identifier: CA2580089360

Gene: IVD

Linked Data

• ClinVar Variation Id: 1725997
• ClinVar RCV Id: RCV002306968

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40407976del , CM000677.2:g.40407976del	GRCh38
NC_000015.9:g.40700175del , CM000677.1:g.40700175del	GRCh37
NC_000015.8:g.38487467del	NCBI36
NG_011986.1:g.7490del
NG_011986.2:g.7492del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000479013.7:c.182del	ENSP00000417990.3:p.Gly61AlafsTer21
ENST00000487418.8:c.272del MANE Select	ENSP00000418397.3:p.Gly91AlafsTer21
ENST00000610693.5:c.359del	ENSP00000479359.2:p.Gly120AlafsTer21
ENST00000650656.1:c.191del	ENSP00000498731.1:p.Gly64AlafsTer21
ENST00000651168.1:c.281del	ENSP00000499074.1:p.Gly94AlafsTer21
ENST00000473112.6:c.31del
ENST00000479013.6:c.191del	ENSP00000417990.2:p.Gly64AlafsTer21
ENST00000487418.6:c.281del	ENSP00000418397.2:p.Gly94AlafsTer21
ENST00000558610.5:c.224del	ENSP00000453821.1:p.Gly75AlafsTer21
ENST00000610693.4:c.368del	ENSP00000479359.1:p.Gly123AlafsTer21
NM_001159508.1:c.191del	NP_001152980.1:p.Gly64AlafsTer21
NM_002225.3:c.281del	NP_002216.2:p.Gly94AlafsTer21
XM_005254350.2:c.281del	XP_005254407.1:p.Gly94AlafsTer21
XM_005254356.2:c.281del	XP_005254413.1:p.Gly94AlafsTer21
XM_006720491.2:c.224del	XP_006720554.1:p.Gly75AlafsTer21
XM_006720492.2:c.281del	XP_006720555.1:p.Gly94AlafsTer21
XM_006720493.2:c.281del	XP_006720556.1:p.Gly94AlafsTer21
XM_006720494.2:c.281del	XP_006720557.1:p.Gly94AlafsTer21
XM_006720495.2:c.281del	XP_006720558.1:p.Gly94AlafsTer21
XM_011521523.1:c.281del	XP_011519825.1:p.Gly94AlafsTer21
XM_011521524.1:c.281del	XP_011519826.1:p.Gly94AlafsTer21
XR_243097.3:n.281del
XR_243098.2:n.281del
XR_429453.2:n.382del
NM_001159508.2:c.182del	NP_001152980.2:p.Gly61AlafsTer21
NM_001354597.2:c.224del	NP_001341526.1:p.Gly75AlafsTer21
NM_001354598.2:c.272del	NP_001341527.2:p.Gly91AlafsTer21
NM_001354599.2:c.359del	NP_001341528.2:p.Gly120AlafsTer21
NM_001354600.2:c.359del	NP_001341529.2:p.Gly120AlafsTer21
NM_001354601.2:c.272del	NP_001341530.2:p.Gly91AlafsTer21
NM_002225.4:c.272del	NP_002216.3:p.Gly91AlafsTer21
NR_148925.1:n.682del
XM_006720495.3:c.281del	XP_006720558.1:p.Gly94AlafsTer21
XM_017022149.1:c.368del	XP_016877638.1:p.Gly123AlafsTer21
XM_017022150.1:c.368del	XP_016877639.1:p.Gly123AlafsTer21
XM_017022153.1:c.368del	XP_016877642.1:p.Gly123AlafsTer21
XM_017022154.2:c.311del	XP_016877643.1:p.Gly104AlafsTer21
XM_017022155.2:c.368del	XP_016877644.1:p.Gly123AlafsTer21
XM_017022157.1:c.368del	XP_016877646.1:p.Gly123AlafsTer21
XM_017022158.2:c.368del	XP_016877647.1:p.Gly123AlafsTer21
XR_001751263.1:n.631del
XR_001751264.1:n.672del
NM_001159508.3:c.182del	NP_001152980.2:p.Gly61AlafsTer21
NM_001354597.3:c.224del	NP_001341526.1:p.Gly75AlafsTer21
NM_001354598.3:c.272del	NP_001341527.2:p.Gly91AlafsTer21
NM_001354599.3:c.359del	NP_001341528.2:p.Gly120AlafsTer21
NM_001354600.3:c.359del	NP_001341529.2:p.Gly120AlafsTer21
NM_001354601.3:c.272del	NP_001341530.2:p.Gly91AlafsTer21
NM_002225.5:c.272del MANE Select	NP_002216.3:p.Gly91AlafsTer21
NR_148925.2:n.684del