Canonical Allele Identifier: CA321927027
Gene: COL18A1 HGNC NCBI
SLC19A1 HGNC NCBI

Linked Data

dbSNP Id: rs1010947180

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45511800_45511802del , CM000683.2:g.45511800_45511802del GRCh38
NC_000021.8:g.46931714_46931716del , CM000683.1:g.46931714_46931716del GRCh37
NC_000021.7:g.45756142_45756144del NCBI36
NG_011903.1:g.111609_111611del
NG_028278.2:g.56344_56346del

Transcript Alleles

HGVS Amino-acid change
ENST00000355480.10:c.4350-388_4350-386del (COL18A1) ENSP00000347665.5:n.4350-388_4350-386del
ENST00000651438.1:c.3810-388_3810-386del (COL18A1) MANE Select ENSP00000498485.1:n.3810-388_3810-386del
ENST00000342220.9:c.1854-388_1854-386del (COL18A1) ENSP00000339118.5:n.1854-388_1854-386del
ENST00000355480.9:c.4350-388_4350-386del (COL18A1) ENSP00000347665.5:n.4350-388_4350-386del
ENST00000359759.8:c.5055-388_5055-386del (COL18A1) ENSP00000352798.4:n.5055-388_5055-386del
ENST00000400337.6:c.3810-388_3810-386del (COL18A1) ENSP00000383191.2:n.3810-388_3810-386del
ENST00000417954.5:c.498-13188_498-13186del (SLC19A1)
ENST00000423214.1:c.764-388_764-386del (COL18A1)
ENST00000473212.1:n.2136-388_2136-386del (COL18A1)
ENST00000567670.5:c.1294-13188_1294-13186del (SLC19A1) ENSP00000457278.1:n.1294-13188_1294-13186...
NM_030582.3:c.4341-388_4341-386del (COL18A1) NP_085059.2:n.4341-388_4341-386del
NM_130444.2:c.5046-388_5046-386del (COL18A1) NP_569711.2:n.5046-388_5046-386del
NM_130445.3:c.3801-388_3801-386del (COL18A1) NP_569712.2:n.3801-388_3801-386del
XM_011529707.1:c.1585-8831_1585-8829del (SLC19A1) XP_011528009.1:n.1585-8831_1585-8829del
XM_017028445.2:c.1585-8831_1585-8829del (SLC19A1) XP_016883934.1:n.1585-8831_1585-8829del
NM_030582.4:c.4341-388_4341-386del (COL18A1) NP_085059.2:n.4341-388_4341-386del
NM_130444.3:c.5046-388_5046-386del (COL18A1) NP_569711.2:n.5046-388_5046-386del
NM_130445.4:c.3801-388_3801-386del (COL18A1) NP_569712.2:n.3801-388_3801-386del
NM_001379500.1:c.3810-388_3810-386del (COL18A1) MANE Select NP_001366429.1:n.3810-388_3810-386del