Canonical Allele Identifier: CA2392191208
Gene: COL18A1 HGNC NCBI
SLC19A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45505163_45505223delinsGCCCGGCCCACCTGGACCTCAGGGACCCCCCGGCATCGGCTACGAGGGGCGCCAGGGCCCT , CM000683.2:g.45505163_45505223delinsGCCCGGCCCACCTGGACCTCAGGGACCCCCCGGCATCGGCTACGAGGGGCGCCAGGGCCCT GRCh38
NC_000021.8:g.46925077_46925137delinsGCCCGGCCCACCTGGACCTCAGGGACCCCCCGGCATCGGCTACGAGGGGCGCCAGGGCCCT , CM000683.1:g.46925077_46925137delinsGCCCGGCCCACCTGGACCTCAGGGACCCCCCGGCATCGGCTACGAGGGGCGCCAGGGCCCT GRCh37
NC_000021.7:g.45749505_45749565delinsGCCCGGCCCACCTGGACCTCAGGGACCCCCCGGCATCGGCTACGAGGGGCGCCAGGGCCCT NCBI36
NG_011903.1:g.104972_105032delinsGCCCGGCCCACCTGGACCTCAGGGACCCCCCGGCATCGGCTACGAGGGGCGCCAGGGCCCT
NG_028278.2:g.62921_62981delinsAGGGCCCTGGCGCCCCTCGTAGCCGATGCCGGGGGGTCCCTGAGGTCCAGGTGGGCCGGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000355480.10:c.3438_3498delinsGCCCGGCCCACCTGGACCTCAGGGACCCCCCGGCATCGGCTACGAGGGGCGCCAGGGCCCT (COL18A1) ENSP00000347665.5:p.Gln1146=
ENST00000651438.1:c.2898_2958delinsGCCCGGCCCACCTGGACCTCAGGGACCCCCCGGCATCGGCTACGAGGGGCGCCAGGGCCCT (COL18A1) MANE Select ENSP00000498485.1:p.Gln966=
ENST00000342220.9:c.939_999delinsGCCCGGCCCACCTGGACCTCAGGGACCCCCCGGCATCGGCTACGAGGGGCGCCAGGGCCCT (COL18A1) ENSP00000339118.5:p.Gln313=
ENST00000355480.9:c.3438_3498delinsGCCCGGCCCACCTGGACCTCAGGGACCCCCCGGCATCGGCTACGAGGGGCGCCAGGGCCCT (COL18A1) ENSP00000347665.5:p.Gln1146=
ENST00000359759.8:c.4143_4203delinsGCCCGGCCCACCTGGACCTCAGGGACCCCCCGGCATCGGCTACGAGGGGCGCCAGGGCCCT (COL18A1) ENSP00000352798.4:p.Gln1381=
ENST00000400337.6:c.2898_2958delinsGCCCGGCCCACCTGGACCTCAGGGACCCCCCGGCATCGGCTACGAGGGGCGCCAGGGCCCT (COL18A1) ENSP00000383191.2:p.Gln966=
ENST00000417954.5:c.498-6611_498-6551delinsAGGGCCCTGGCGCCCCTCGTAGCCGATGCCGGGGGGTCCCTGAGGTCCAGGTGGGCCGGGC (SLC19A1)
ENST00000567670.5:c.1294-6611_1294-6551delinsAGGGCCCTGGCGCCCCTCGTAGCCGATGCCGGGGGGTCCCTGAGGTCCAGGTGGGCCGGGC (SLC19A1) ENSP00000457278.1:n.1294-6611_1294-6551delinsAGGGCCCTGGCGCCCC...
NM_030582.3:c.3429_3489delinsGCCCGGCCCACCTGGACCTCAGGGACCCCCCGGCATCGGCTACGAGGGGCGCCAGGGCCCT (COL18A1) NP_085059.2:p.Gln1143=
NM_130444.2:c.4134_4194delinsGCCCGGCCCACCTGGACCTCAGGGACCCCCCGGCATCGGCTACGAGGGGCGCCAGGGCCCT (COL18A1) NP_569711.2:p.Gln1378=
NM_130445.3:c.2889_2949delinsGCCCGGCCCACCTGGACCTCAGGGACCCCCCGGCATCGGCTACGAGGGGCGCCAGGGCCCT (COL18A1) NP_569712.2:p.Gln963=
XM_011529707.1:c.1585-2254_1585-2194delinsAGGGCCCTGGCGCCCCTCGTAGCCGATGCCGGGGGGTCCCTGAGGTCCAGGTGGGCCGGGC (SLC19A1) XP_011528009.1:n.1585-2254_1585-2194delinsAGGGCCCTGGCGCCCCTCG...
XM_017028445.2:c.1585-2254_1585-2194delinsAGGGCCCTGGCGCCCCTCGTAGCCGATGCCGGGGGGTCCCTGAGGTCCAGGTGGGCCGGGC (SLC19A1) XP_016883934.1:n.1585-2254_1585-2194delinsAGGGCCCTGGCGCCCCTCG...
NM_030582.4:c.3429_3489delinsGCCCGGCCCACCTGGACCTCAGGGACCCCCCGGCATCGGCTACGAGGGGCGCCAGGGCCCT (COL18A1) NP_085059.2:p.Gln1143=
NM_130444.3:c.4134_4194delinsGCCCGGCCCACCTGGACCTCAGGGACCCCCCGGCATCGGCTACGAGGGGCGCCAGGGCCCT (COL18A1) NP_569711.2:p.Gln1378=
NM_130445.4:c.2889_2949delinsGCCCGGCCCACCTGGACCTCAGGGACCCCCCGGCATCGGCTACGAGGGGCGCCAGGGCCCT (COL18A1) NP_569712.2:p.Gln963=
NM_001379500.1:c.2898_2958delinsGCCCGGCCCACCTGGACCTCAGGGACCCCCCGGCATCGGCTACGAGGGGCGCCAGGGCCCT (COL18A1) MANE Select NP_001366429.1:p.Gln966=