Canonical Allele Identifier: CA2627815008
Gene: IVD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40411415_40411416insTCT , CM000677.2:g.40411415_40411416insTCT GRCh38
NC_000015.9:g.40703614_40703615insTCT , CM000677.1:g.40703614_40703615insTCT GRCh37
NC_000015.8:g.38490906_38490907insTCT NCBI36
NG_011986.1:g.10929_10930insTCT
NG_011986.2:g.10931_10932insTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000479013.7:c.460+62_460+63insTCT ENSP00000417990.3:n.460+62_460+63insTCT
ENST00000487418.8:c.550+62_550+63insTCT MANE Select ENSP00000418397.3:n.550+62_550+63insTCT
ENST00000650656.1:c.469+62_469+63insTCT ENSP00000498731.1:n.469+62_469+63insTCT
ENST00000651168.1:c.559+62_559+63insTCT ENSP00000499074.1:n.559+62_559+63insTCT
ENST00000473112.6:c.309+62_309+63insTCT
ENST00000479013.6:c.469+62_469+63insTCT ENSP00000417990.2:n.469+62_469+63insTCT
ENST00000481262.6:c.156+62_156+63insTCT
ENST00000484250.1:n.173+62_173+63insTCT
ENST00000487418.6:c.559+62_559+63insTCT ENSP00000418397.2:n.559+62_559+63insTCT
ENST00000558610.5:c.502+62_502+63insTCT ENSP00000453821.1:n.502+62_502+63insTCT
NM_001159508.1:c.469+62_469+63insTCT NP_001152980.1:n.469+62_469+63insTCT
NM_002225.3:c.559+62_559+63insTCT NP_002216.2:n.559+62_559+63insTCT
XM_005254350.2:c.559+62_559+63insTCT XP_005254407.1:n.559+62_559+63insTCT
XM_005254356.2:c.559+62_559+63insTCT XP_005254413.1:n.559+62_559+63insTCT
XM_006720491.2:c.502+62_502+63insTCT XP_006720554.1:n.502+62_502+63insTCT
XM_006720492.2:c.559+62_559+63insTCT XP_006720555.1:n.559+62_559+63insTCT
XM_006720493.2:c.559+62_559+63insTCT XP_006720556.1:n.559+62_559+63insTCT
XM_006720494.2:c.559+62_559+63insTCT XP_006720557.1:n.559+62_559+63insTCT
XM_006720495.2:c.559+62_559+63insTCT XP_006720558.1:n.559+62_559+63insTCT
XM_011521523.1:c.559+62_559+63insTCT XP_011519825.1:n.559+62_559+63insTCT
XM_011521524.1:c.559+62_559+63insTCT XP_011519826.1:n.559+62_559+63insTCT
XR_243097.3:n.559+62_559+63insTCT
XR_243098.2:n.559+62_559+63insTCT
XR_429453.2:n.660+62_660+63insTCT
NM_001159508.2:c.460+62_460+63insTCT NP_001152980.2:n.460+62_460+63insTCT
NM_001354597.2:c.502+62_502+63insTCT NP_001341526.1:n.502+62_502+63insTCT
NM_001354598.2:c.550+62_550+63insTCT NP_001341527.2:n.550+62_550+63insTCT
NM_001354599.2:c.637+62_637+63insTCT NP_001341528.2:n.637+62_637+63insTCT
NM_001354600.2:c.637+62_637+63insTCT NP_001341529.2:n.637+62_637+63insTCT
NM_001354601.2:c.550+62_550+63insTCT NP_001341530.2:n.550+62_550+63insTCT
NM_002225.4:c.550+62_550+63insTCT NP_002216.3:n.550+62_550+63insTCT
NR_148925.1:n.960+62_960+63insTCT
XM_006720495.3:c.559+62_559+63insTCT XP_006720558.1:n.559+62_559+63insTCT
XM_017022149.1:c.646+62_646+63insTCT XP_016877638.1:n.646+62_646+63insTCT
XM_017022150.1:c.646+62_646+63insTCT XP_016877639.1:n.646+62_646+63insTCT
XM_017022153.1:c.646+62_646+63insTCT XP_016877642.1:n.646+62_646+63insTCT
XM_017022154.2:c.589+62_589+63insTCT XP_016877643.1:n.589+62_589+63insTCT
XM_017022155.2:c.646+62_646+63insTCT XP_016877644.1:n.646+62_646+63insTCT
XM_017022157.1:c.646+62_646+63insTCT XP_016877646.1:n.646+62_646+63insTCT
XM_017022158.2:c.646+62_646+63insTCT XP_016877647.1:n.646+62_646+63insTCT
XR_001751263.1:n.909+62_909+63insTCT
XR_001751264.1:n.950+62_950+63insTCT
NM_001159508.3:c.460+62_460+63insTCT NP_001152980.2:n.460+62_460+63insTCT
NM_001354597.3:c.502+62_502+63insTCT NP_001341526.1:n.502+62_502+63insTCT
NM_001354598.3:c.550+62_550+63insTCT NP_001341527.2:n.550+62_550+63insTCT
NM_001354599.3:c.637+62_637+63insTCT NP_001341528.2:n.637+62_637+63insTCT
NM_001354600.3:c.637+62_637+63insTCT NP_001341529.2:n.637+62_637+63insTCT
NM_001354601.3:c.550+62_550+63insTCT NP_001341530.2:n.550+62_550+63insTCT
NM_002225.5:c.550+62_550+63insTCT MANE Select NP_002216.3:n.550+62_550+63insTCT
NR_148925.2:n.962+62_962+63insTCT