Canonical Allele Identifier: CA2740094755
Gene: COL18A1 HGNC NCBI
SLC19A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3053786
ClinVar RCV Id: RCV003964289

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45505247_45505255dup , CM000683.2:g.45505247_45505255dup GRCh38
NC_000021.8:g.46925161_46925169dup , CM000683.1:g.46925161_46925169dup GRCh37
NC_000021.7:g.45749589_45749597dup NCBI36
NG_011903.1:g.105056_105064dup
NG_028278.2:g.62889_62897dup

Transcript Alleles

HGVS Amino-acid change
ENST00000355480.10:c.3522_3530dup (COL18A1) ENSP00000347665.5:p.Ser1177_Phe1178insPro...
ENST00000651438.1:c.2982_2990dup (COL18A1) MANE Select ENSP00000498485.1:p.Ser997_Phe998insProPr...
ENST00000342220.9:c.1023_1031dup (COL18A1) ENSP00000339118.5:p.Ser344_Phe345insProPr...
ENST00000355480.9:c.3522_3530dup (COL18A1) ENSP00000347665.5:p.Ser1177_Phe1178insPro...
ENST00000359759.8:c.4227_4235dup (COL18A1) ENSP00000352798.4:p.Ser1412_Phe1413insPro...
ENST00000400337.6:c.2982_2990dup (COL18A1) ENSP00000383191.2:p.Ser997_Phe998insProPr...
ENST00000417954.5:c.498-6643_498-6635dup (SLC19A1)
ENST00000567670.5:c.1294-6643_1294-6635dup (SLC19A1) ENSP00000457278.1:n.1294-6643_1294-6635du...
NM_030582.3:c.3513_3521dup (COL18A1) NP_085059.2:p.Ser1174_Phe1175insProProSer...
NM_130444.2:c.4218_4226dup (COL18A1) NP_569711.2:p.Ser1409_Phe1410insProProSer...
NM_130445.3:c.2973_2981dup (COL18A1) NP_569712.2:p.Ser994_Phe995insProProSer
XM_011529707.1:c.1585-2286_1585-2278dup (SLC19A1) XP_011528009.1:n.1585-2286_1585-2278dup
XM_017028445.2:c.1585-2286_1585-2278dup (SLC19A1) XP_016883934.1:n.1585-2286_1585-2278dup
NM_030582.4:c.3513_3521dup (COL18A1) NP_085059.2:p.Ser1174_Phe1175insProProSer...
NM_130444.3:c.4218_4226dup (COL18A1) NP_569711.2:p.Ser1409_Phe1410insProProSer...
NM_130445.4:c.2973_2981dup (COL18A1) NP_569712.2:p.Ser994_Phe995insProProSer
NM_001379500.1:c.2982_2990dup (COL18A1) MANE Select NP_001366429.1:p.Ser997_Phe998insProProSe...