Canonical Allele Identifier: CA2654921929
Gene: COL18A1 HGNC NCBI
SLC19A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45511221del , CM000683.2:g.45511221del GRCh38
NC_000021.8:g.46931135del , CM000683.1:g.46931135del GRCh37
NC_000021.7:g.45755563del NCBI36
NG_011903.1:g.111030del
NG_028278.2:g.56926del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355480.10:c.4344del (COL18A1) ENSP00000347665.5:p.Thr1449ProfsTer18
ENST00000651438.1:c.3804del (COL18A1) MANE Select ENSP00000498485.1:p.Thr1269ProfsTer18
ENST00000342220.9:c.1848del (COL18A1) ENSP00000339118.5:p.Thr617ProfsTer18
ENST00000355480.9:c.4344del (COL18A1) ENSP00000347665.5:p.Thr1449ProfsTer18
ENST00000359759.8:c.5049del (COL18A1) ENSP00000352798.4:p.Thr1684ProfsTer18
ENST00000400337.6:c.3804del (COL18A1) ENSP00000383191.2:p.Thr1269ProfsTer18
ENST00000417954.5:c.498-12606del (SLC19A1)
ENST00000423214.1:c.758del (COL18A1)
ENST00000473212.1:n.2130del (COL18A1)
ENST00000567670.5:c.1294-12606del (SLC19A1) ENSP00000457278.1:n.1294-12606del
NM_030582.3:c.4335del (COL18A1) NP_085059.2:p.Thr1446ProfsTer18
NM_130444.2:c.5040del (COL18A1) NP_569711.2:p.Thr1681ProfsTer18
NM_130445.3:c.3795del (COL18A1) NP_569712.2:p.Thr1266ProfsTer18
XM_011529707.1:c.1585-8249del (SLC19A1) XP_011528009.1:n.1585-8249del
XM_017028445.2:c.1585-8249del (SLC19A1) XP_016883934.1:n.1585-8249del
NM_030582.4:c.4335del (COL18A1) NP_085059.2:p.Thr1446ProfsTer18
NM_130444.3:c.5040del (COL18A1) NP_569711.2:p.Thr1681ProfsTer18
NM_130445.4:c.3795del (COL18A1) NP_569712.2:p.Thr1266ProfsTer18
NM_001379500.1:c.3804del (COL18A1) MANE Select NP_001366429.1:p.Thr1269ProfsTer18