Canonical Allele Identifier: CA2171764337
Gene: IVD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40408097_40408098delinsGA , CM000677.2:g.40408097_40408098delinsGA GRCh38
NC_000015.9:g.40700296_40700297delinsGA , CM000677.1:g.40700296_40700297delinsGA GRCh37
NC_000015.8:g.38487588_38487589delinsGA NCBI36
NG_011986.1:g.7611_7612delinsGA
NG_011986.2:g.7613_7614delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000479013.7:c.196+107_196+108delinsGA ENSP00000417990.3:n.196+107_196+108delinsGA
ENST00000487418.8:c.286+107_286+108delinsGA MANE Select ENSP00000418397.3:n.286+107_286+108delinsGA
ENST00000610693.5:c.373+107_373+108delinsGA ENSP00000479359.2:n.373+107_373+108delinsGA
ENST00000650656.1:c.205+107_205+108delinsGA ENSP00000498731.1:n.205+107_205+108delinsGA
ENST00000651168.1:c.295+107_295+108delinsGA ENSP00000499074.1:n.295+107_295+108delinsGA
ENST00000473112.6:c.45+107_45+108delinsGA
ENST00000479013.6:c.205+107_205+108delinsGA ENSP00000417990.2:n.205+107_205+108delinsGA
ENST00000487418.6:c.295+107_295+108delinsGA ENSP00000418397.2:n.295+107_295+108delinsGA
ENST00000558610.5:c.238+107_238+108delinsGA ENSP00000453821.1:n.238+107_238+108delinsGA
ENST00000610693.4:c.382+107_382+108delinsGA ENSP00000479359.1:n.382+107_382+108delinsGA
NM_001159508.1:c.205+107_205+108delinsGA NP_001152980.1:n.205+107_205+108delinsGA
NM_002225.3:c.295+107_295+108delinsGA NP_002216.2:n.295+107_295+108delinsGA
XM_005254350.2:c.295+107_295+108delinsGA XP_005254407.1:n.295+107_295+108delinsGA
XM_005254356.2:c.295+107_295+108delinsGA XP_005254413.1:n.295+107_295+108delinsGA
XM_006720491.2:c.238+107_238+108delinsGA XP_006720554.1:n.238+107_238+108delinsGA
XM_006720492.2:c.295+107_295+108delinsGA XP_006720555.1:n.295+107_295+108delinsGA
XM_006720493.2:c.295+107_295+108delinsGA XP_006720556.1:n.295+107_295+108delinsGA
XM_006720494.2:c.295+107_295+108delinsGA XP_006720557.1:n.295+107_295+108delinsGA
XM_006720495.2:c.295+107_295+108delinsGA XP_006720558.1:n.295+107_295+108delinsGA
XM_011521523.1:c.295+107_295+108delinsGA XP_011519825.1:n.295+107_295+108delinsGA
XM_011521524.1:c.295+107_295+108delinsGA XP_011519826.1:n.295+107_295+108delinsGA
XR_243097.3:n.295+107_295+108delinsGA
XR_243098.2:n.295+107_295+108delinsGA
XR_429453.2:n.396+107_396+108delinsGA
NM_001159508.2:c.196+107_196+108delinsGA NP_001152980.2:n.196+107_196+108delinsGA
NM_001354597.2:c.238+107_238+108delinsGA NP_001341526.1:n.238+107_238+108delinsGA
NM_001354598.2:c.286+107_286+108delinsGA NP_001341527.2:n.286+107_286+108delinsGA
NM_001354599.2:c.373+107_373+108delinsGA NP_001341528.2:n.373+107_373+108delinsGA
NM_001354600.2:c.373+107_373+108delinsGA NP_001341529.2:n.373+107_373+108delinsGA
NM_001354601.2:c.286+107_286+108delinsGA NP_001341530.2:n.286+107_286+108delinsGA
NM_002225.4:c.286+107_286+108delinsGA NP_002216.3:n.286+107_286+108delinsGA
NR_148925.1:n.696+107_696+108delinsGA
XM_006720495.3:c.295+107_295+108delinsGA XP_006720558.1:n.295+107_295+108delinsGA
XM_017022149.1:c.382+107_382+108delinsGA XP_016877638.1:n.382+107_382+108delinsGA
XM_017022150.1:c.382+107_382+108delinsGA XP_016877639.1:n.382+107_382+108delinsGA
XM_017022153.1:c.382+107_382+108delinsGA XP_016877642.1:n.382+107_382+108delinsGA
XM_017022154.2:c.325+107_325+108delinsGA XP_016877643.1:n.325+107_325+108delinsGA
XM_017022155.2:c.382+107_382+108delinsGA XP_016877644.1:n.382+107_382+108delinsGA
XM_017022157.1:c.382+107_382+108delinsGA XP_016877646.1:n.382+107_382+108delinsGA
XM_017022158.2:c.382+107_382+108delinsGA XP_016877647.1:n.382+107_382+108delinsGA
XR_001751263.1:n.645+107_645+108delinsGA
XR_001751264.1:n.686+107_686+108delinsGA
NM_001159508.3:c.196+107_196+108delinsGA NP_001152980.2:n.196+107_196+108delinsGA
NM_001354597.3:c.238+107_238+108delinsGA NP_001341526.1:n.238+107_238+108delinsGA
NM_001354598.3:c.286+107_286+108delinsGA NP_001341527.2:n.286+107_286+108delinsGA
NM_001354599.3:c.373+107_373+108delinsGA NP_001341528.2:n.373+107_373+108delinsGA
NM_001354600.3:c.373+107_373+108delinsGA NP_001341529.2:n.373+107_373+108delinsGA
NM_001354601.3:c.286+107_286+108delinsGA NP_001341530.2:n.286+107_286+108delinsGA
NM_002225.5:c.286+107_286+108delinsGA MANE Select NP_002216.3:n.286+107_286+108delinsGA
NR_148925.2:n.698+107_698+108delinsGA