Canonical Allele Identifier: CA2392196314
Gene: COL18A1 HGNC NCBI
SLC19A1 HGNC NCBI

Linked Data

dbSNP Id: rs2037629370

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45511838_45511852del , CM000683.2:g.45511838_45511852del GRCh38
NC_000021.8:g.46931752_46931766del , CM000683.1:g.46931752_46931766del GRCh37
NC_000021.7:g.45756180_45756194del NCBI36
NG_011903.1:g.111647_111661del
NG_028278.2:g.56293_56307del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355480.10:c.4350-350_4350-336del (COL18A1) ENSP00000347665.5:n.4350-350_4350-336del
ENST00000651438.1:c.3810-350_3810-336del (COL18A1) MANE Select ENSP00000498485.1:n.3810-350_3810-336del
ENST00000342220.9:c.1854-350_1854-336del (COL18A1) ENSP00000339118.5:n.1854-350_1854-336del
ENST00000355480.9:c.4350-350_4350-336del (COL18A1) ENSP00000347665.5:n.4350-350_4350-336del
ENST00000359759.8:c.5055-350_5055-336del (COL18A1) ENSP00000352798.4:n.5055-350_5055-336del
ENST00000400337.6:c.3810-350_3810-336del (COL18A1) ENSP00000383191.2:n.3810-350_3810-336del
ENST00000417954.5:c.498-13239_498-13225del (SLC19A1)
ENST00000423214.1:c.764-350_764-336del (COL18A1)
ENST00000473212.1:n.2136-350_2136-336del (COL18A1)
ENST00000567670.5:c.1294-13239_1294-13225del (SLC19A1) ENSP00000457278.1:n.1294-13239_1294-13225del
NM_030582.3:c.4341-350_4341-336del (COL18A1) NP_085059.2:n.4341-350_4341-336del
NM_130444.2:c.5046-350_5046-336del (COL18A1) NP_569711.2:n.5046-350_5046-336del
NM_130445.3:c.3801-350_3801-336del (COL18A1) NP_569712.2:n.3801-350_3801-336del
XM_011529707.1:c.1585-8882_1585-8868del (SLC19A1) XP_011528009.1:n.1585-8882_1585-8868del
XM_017028445.2:c.1585-8882_1585-8868del (SLC19A1) XP_016883934.1:n.1585-8882_1585-8868del
NM_030582.4:c.4341-350_4341-336del (COL18A1) NP_085059.2:n.4341-350_4341-336del
NM_130444.3:c.5046-350_5046-336del (COL18A1) NP_569711.2:n.5046-350_5046-336del
NM_130445.4:c.3801-350_3801-336del (COL18A1) NP_569712.2:n.3801-350_3801-336del
NM_001379500.1:c.3810-350_3810-336del (COL18A1) MANE Select NP_001366429.1:n.3810-350_3810-336del