Canonical Allele Identifier: CA2171765950
Gene: IVD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40411601C= , CM000677.2:g.40411601C= GRCh38
NC_000015.9:g.40703800C= , CM000677.1:g.40703800C= GRCh37
NC_000015.8:g.38491092C= NCBI36
NG_011986.1:g.11115C=
NG_011986.2:g.11117C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000479013.7:c.507C= ENSP00000417990.3:p.Gly169=
ENST00000487418.8:c.597C= MANE Select ENSP00000418397.3:p.Gly199=
ENST00000650656.1:c.516C= ENSP00000498731.1:p.Gly172=
ENST00000651168.1:c.606C= ENSP00000499074.1:p.Gly202=
ENST00000473112.6:c.356C=
ENST00000479013.6:c.516C= ENSP00000417990.2:p.Gly172=
ENST00000481262.6:c.203C=
ENST00000484250.1:n.220C=
ENST00000487418.6:c.606C= ENSP00000418397.2:p.Gly202=
ENST00000558610.5:c.549C= ENSP00000453821.1:p.Gly183=
NM_001159508.1:c.516C= NP_001152980.1:p.Gly172=
NM_002225.3:c.606C= NP_002216.2:p.Gly202=
XM_005254350.2:c.606C= XP_005254407.1:p.Gly202=
XM_005254356.2:c.606C= XP_005254413.1:p.Gly202=
XM_006720491.2:c.549C= XP_006720554.1:p.Gly183=
XM_006720492.2:c.606C= XP_006720555.1:p.Gly202=
XM_006720493.2:c.606C= XP_006720556.1:p.Gly202=
XM_006720494.2:c.606C= XP_006720557.1:p.Gly202=
XM_006720495.2:c.606C= XP_006720558.1:p.Gly202=
XM_011521523.1:c.606C= XP_011519825.1:p.Gly202=
XM_011521524.1:c.606C= XP_011519826.1:p.Gly202=
XR_243097.3:n.606C=
XR_243098.2:n.606C=
XR_429453.2:n.707C=
NM_001159508.2:c.507C= NP_001152980.2:p.Gly169=
NM_001354597.2:c.549C= NP_001341526.1:p.Gly183=
NM_001354598.2:c.597C= NP_001341527.2:p.Gly199=
NM_001354599.2:c.684C= NP_001341528.2:p.Gly228=
NM_001354600.2:c.684C= NP_001341529.2:p.Gly228=
NM_001354601.2:c.597C= NP_001341530.2:p.Gly199=
NM_002225.4:c.597C= NP_002216.3:p.Gly199=
NR_148925.1:n.1007C=
XM_006720495.3:c.606C= XP_006720558.1:p.Gly202=
XM_017022149.1:c.693C= XP_016877638.1:p.Gly231=
XM_017022150.1:c.693C= XP_016877639.1:p.Gly231=
XM_017022153.1:c.693C= XP_016877642.1:p.Gly231=
XM_017022154.2:c.636C= XP_016877643.1:p.Gly212=
XM_017022155.2:c.693C= XP_016877644.1:p.Gly231=
XM_017022157.1:c.693C= XP_016877646.1:p.Gly231=
XM_017022158.2:c.693C= XP_016877647.1:p.Gly231=
XR_001751263.1:n.956C=
XR_001751264.1:n.997C=
NM_001159508.3:c.507C= NP_001152980.2:p.Gly169=
NM_001354597.3:c.549C= NP_001341526.1:p.Gly183=
NM_001354598.3:c.597C= NP_001341527.2:p.Gly199=
NM_001354599.3:c.684C= NP_001341528.2:p.Gly228=
NM_001354600.3:c.684C= NP_001341529.2:p.Gly228=
NM_001354601.3:c.597C= NP_001341530.2:p.Gly199=
NM_002225.5:c.597C= MANE Select NP_002216.3:p.Gly199=
NR_148925.2:n.1009C=