Canonical Allele Identifier: CA2171765877

Gene: IVD

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40411434_40411435delinsGC , CM000677.2:g.40411434_40411435delinsGC	GRCh38
NC_000015.9:g.40703633_40703634delinsGC , CM000677.1:g.40703633_40703634delinsGC	GRCh37
NC_000015.8:g.38490925_38490926delinsGC	NCBI36
NG_011986.1:g.10948_10949delinsGC
NG_011986.2:g.10950_10951delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000479013.7:c.460+81_460+82delinsGC	ENSP00000417990.3:n.460+81_460+82delinsGC
ENST00000487418.8:c.550+81_550+82delinsGC MANE Select	ENSP00000418397.3:n.550+81_550+82delinsGC
ENST00000650656.1:c.469+81_469+82delinsGC	ENSP00000498731.1:n.469+81_469+82delinsGC
ENST00000651168.1:c.559+81_559+82delinsGC	ENSP00000499074.1:n.559+81_559+82delinsGC
ENST00000473112.6:c.309+81_309+82delinsGC
ENST00000479013.6:c.469+81_469+82delinsGC	ENSP00000417990.2:n.469+81_469+82delinsGC
ENST00000481262.6:c.156+81_156+82delinsGC
ENST00000484250.1:n.173+81_173+82delinsGC
ENST00000487418.6:c.559+81_559+82delinsGC	ENSP00000418397.2:n.559+81_559+82delinsGC
ENST00000558610.5:c.502+81_502+82delinsGC	ENSP00000453821.1:n.502+81_502+82delinsGC
NM_001159508.1:c.469+81_469+82delinsGC	NP_001152980.1:n.469+81_469+82delinsGC
NM_002225.3:c.559+81_559+82delinsGC	NP_002216.2:n.559+81_559+82delinsGC
XM_005254350.2:c.559+81_559+82delinsGC	XP_005254407.1:n.559+81_559+82delinsGC
XM_005254356.2:c.559+81_559+82delinsGC	XP_005254413.1:n.559+81_559+82delinsGC
XM_006720491.2:c.502+81_502+82delinsGC	XP_006720554.1:n.502+81_502+82delinsGC
XM_006720492.2:c.559+81_559+82delinsGC	XP_006720555.1:n.559+81_559+82delinsGC
XM_006720493.2:c.559+81_559+82delinsGC	XP_006720556.1:n.559+81_559+82delinsGC
XM_006720494.2:c.559+81_559+82delinsGC	XP_006720557.1:n.559+81_559+82delinsGC
XM_006720495.2:c.559+81_559+82delinsGC	XP_006720558.1:n.559+81_559+82delinsGC
XM_011521523.1:c.559+81_559+82delinsGC	XP_011519825.1:n.559+81_559+82delinsGC
XM_011521524.1:c.559+81_559+82delinsGC	XP_011519826.1:n.559+81_559+82delinsGC
XR_243097.3:n.559+81_559+82delinsGC
XR_243098.2:n.559+81_559+82delinsGC
XR_429453.2:n.660+81_660+82delinsGC
NM_001159508.2:c.460+81_460+82delinsGC	NP_001152980.2:n.460+81_460+82delinsGC
NM_001354597.2:c.502+81_502+82delinsGC	NP_001341526.1:n.502+81_502+82delinsGC
NM_001354598.2:c.550+81_550+82delinsGC	NP_001341527.2:n.550+81_550+82delinsGC
NM_001354599.2:c.637+81_637+82delinsGC	NP_001341528.2:n.637+81_637+82delinsGC
NM_001354600.2:c.637+81_637+82delinsGC	NP_001341529.2:n.637+81_637+82delinsGC
NM_001354601.2:c.550+81_550+82delinsGC	NP_001341530.2:n.550+81_550+82delinsGC
NM_002225.4:c.550+81_550+82delinsGC	NP_002216.3:n.550+81_550+82delinsGC
NR_148925.1:n.960+81_960+82delinsGC
XM_006720495.3:c.559+81_559+82delinsGC	XP_006720558.1:n.559+81_559+82delinsGC
XM_017022149.1:c.646+81_646+82delinsGC	XP_016877638.1:n.646+81_646+82delinsGC
XM_017022150.1:c.646+81_646+82delinsGC	XP_016877639.1:n.646+81_646+82delinsGC
XM_017022153.1:c.646+81_646+82delinsGC	XP_016877642.1:n.646+81_646+82delinsGC
XM_017022154.2:c.589+81_589+82delinsGC	XP_016877643.1:n.589+81_589+82delinsGC
XM_017022155.2:c.646+81_646+82delinsGC	XP_016877644.1:n.646+81_646+82delinsGC
XM_017022157.1:c.646+81_646+82delinsGC	XP_016877646.1:n.646+81_646+82delinsGC
XM_017022158.2:c.646+81_646+82delinsGC	XP_016877647.1:n.646+81_646+82delinsGC
XR_001751263.1:n.909+81_909+82delinsGC
XR_001751264.1:n.950+81_950+82delinsGC
NM_001159508.3:c.460+81_460+82delinsGC	NP_001152980.2:n.460+81_460+82delinsGC
NM_001354597.3:c.502+81_502+82delinsGC	NP_001341526.1:n.502+81_502+82delinsGC
NM_001354598.3:c.550+81_550+82delinsGC	NP_001341527.2:n.550+81_550+82delinsGC
NM_001354599.3:c.637+81_637+82delinsGC	NP_001341528.2:n.637+81_637+82delinsGC
NM_001354600.3:c.637+81_637+82delinsGC	NP_001341529.2:n.637+81_637+82delinsGC
NM_001354601.3:c.550+81_550+82delinsGC	NP_001341530.2:n.550+81_550+82delinsGC
NM_002225.5:c.550+81_550+82delinsGC MANE Select	NP_002216.3:n.550+81_550+82delinsGC
NR_148925.2:n.962+81_962+82delinsGC