Canonical Allele Identifier: CA2171765846
Gene: IVD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40411371T= , CM000677.2:g.40411371T= GRCh38
NC_000015.9:g.40703570T= , CM000677.1:g.40703570T= GRCh37
NC_000015.8:g.38490862T= NCBI36
NG_011986.1:g.10885T=
NG_011986.2:g.10887T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000479013.7:c.460+18T= ENSP00000417990.3:n.460+18T=
ENST00000487418.8:c.550+18T= MANE Select ENSP00000418397.3:n.550+18T=
ENST00000650656.1:c.469+18T= ENSP00000498731.1:n.469+18T=
ENST00000651168.1:c.559+18T= ENSP00000499074.1:n.559+18T=
ENST00000473112.6:c.309+18T=
ENST00000479013.6:c.469+18T= ENSP00000417990.2:n.469+18T=
ENST00000481262.6:c.156+18T=
ENST00000484250.1:n.173+18T=
ENST00000487418.6:c.559+18T= ENSP00000418397.2:n.559+18T=
ENST00000558610.5:c.502+18T= ENSP00000453821.1:n.502+18T=
NM_001159508.1:c.469+18T= NP_001152980.1:n.469+18T=
NM_002225.3:c.559+18T= NP_002216.2:n.559+18T=
XM_005254350.2:c.559+18T= XP_005254407.1:n.559+18T=
XM_005254356.2:c.559+18T= XP_005254413.1:n.559+18T=
XM_006720491.2:c.502+18T= XP_006720554.1:n.502+18T=
XM_006720492.2:c.559+18T= XP_006720555.1:n.559+18T=
XM_006720493.2:c.559+18T= XP_006720556.1:n.559+18T=
XM_006720494.2:c.559+18T= XP_006720557.1:n.559+18T=
XM_006720495.2:c.559+18T= XP_006720558.1:n.559+18T=
XM_011521523.1:c.559+18T= XP_011519825.1:n.559+18T=
XM_011521524.1:c.559+18T= XP_011519826.1:n.559+18T=
XR_243097.3:n.559+18T=
XR_243098.2:n.559+18T=
XR_429453.2:n.660+18T=
NM_001159508.2:c.460+18T= NP_001152980.2:n.460+18T=
NM_001354597.2:c.502+18T= NP_001341526.1:n.502+18T=
NM_001354598.2:c.550+18T= NP_001341527.2:n.550+18T=
NM_001354599.2:c.637+18T= NP_001341528.2:n.637+18T=
NM_001354600.2:c.637+18T= NP_001341529.2:n.637+18T=
NM_001354601.2:c.550+18T= NP_001341530.2:n.550+18T=
NM_002225.4:c.550+18T= NP_002216.3:n.550+18T=
NR_148925.1:n.960+18T=
XM_006720495.3:c.559+18T= XP_006720558.1:n.559+18T=
XM_017022149.1:c.646+18T= XP_016877638.1:n.646+18T=
XM_017022150.1:c.646+18T= XP_016877639.1:n.646+18T=
XM_017022153.1:c.646+18T= XP_016877642.1:n.646+18T=
XM_017022154.2:c.589+18T= XP_016877643.1:n.589+18T=
XM_017022155.2:c.646+18T= XP_016877644.1:n.646+18T=
XM_017022157.1:c.646+18T= XP_016877646.1:n.646+18T=
XM_017022158.2:c.646+18T= XP_016877647.1:n.646+18T=
XR_001751263.1:n.909+18T=
XR_001751264.1:n.950+18T=
NM_001159508.3:c.460+18T= NP_001152980.2:n.460+18T=
NM_001354597.3:c.502+18T= NP_001341526.1:n.502+18T=
NM_001354598.3:c.550+18T= NP_001341527.2:n.550+18T=
NM_001354599.3:c.637+18T= NP_001341528.2:n.637+18T=
NM_001354600.3:c.637+18T= NP_001341529.2:n.637+18T=
NM_001354601.3:c.550+18T= NP_001341530.2:n.550+18T=
NM_002225.5:c.550+18T= MANE Select NP_002216.3:n.550+18T=
NR_148925.2:n.962+18T=