Canonical Allele Identifier: CA1022830655
Gene: COL18A1 HGNC NCBI
SLC19A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45510951_45511053del , CM000683.2:g.45510951_45511053del GRCh38
NC_000021.8:g.46930865_46930967del , CM000683.1:g.46930865_46930967del GRCh37
NC_000021.7:g.45755293_45755395del NCBI36
NG_011903.1:g.110760_110862del
NG_028278.2:g.57094_57196del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355480.10:c.4234-160_4234-58del (COL18A1) ENSP00000347665.5:n.4234-160_4234-58del
ENST00000651438.1:c.3694-160_3694-58del (COL18A1) MANE Select ENSP00000498485.1:n.3694-160_3694-58del
ENST00000342220.9:c.1738-160_1738-58del (COL18A1) ENSP00000339118.5:n.1738-160_1738-58del
ENST00000355480.9:c.4234-160_4234-58del (COL18A1) ENSP00000347665.5:n.4234-160_4234-58del
ENST00000359759.8:c.4939-160_4939-58del (COL18A1) ENSP00000352798.4:n.4939-160_4939-58del
ENST00000400337.6:c.3694-160_3694-58del (COL18A1) ENSP00000383191.2:n.3694-160_3694-58del
ENST00000417954.5:c.498-12438_498-12336del (SLC19A1)
ENST00000423214.1:c.648-160_648-58del (COL18A1)
ENST00000473212.1:n.2020-160_2020-58del (COL18A1)
ENST00000567670.5:c.1294-12438_1294-12336del (SLC19A1) ENSP00000457278.1:n.1294-12438_1294-12336del
NM_030582.3:c.4225-160_4225-58del (COL18A1) NP_085059.2:n.4225-160_4225-58del
NM_130444.2:c.4930-160_4930-58del (COL18A1) NP_569711.2:n.4930-160_4930-58del
NM_130445.3:c.3685-160_3685-58del (COL18A1) NP_569712.2:n.3685-160_3685-58del
XM_011529707.1:c.1585-8081_1585-7979del (SLC19A1) XP_011528009.1:n.1585-8081_1585-7979del
XM_017028445.2:c.1585-8081_1585-7979del (SLC19A1) XP_016883934.1:n.1585-8081_1585-7979del
NM_030582.4:c.4225-160_4225-58del (COL18A1) NP_085059.2:n.4225-160_4225-58del
NM_130444.3:c.4930-160_4930-58del (COL18A1) NP_569711.2:n.4930-160_4930-58del
NM_130445.4:c.3685-160_3685-58del (COL18A1) NP_569712.2:n.3685-160_3685-58del
NM_001379500.1:c.3694-160_3694-58del (COL18A1) MANE Select NP_001366429.1:n.3694-160_3694-58del