Canonical Allele Identifier: CA410499093
Gene: COL18A1 HGNC NCBI
SLC19A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1469729
ClinVar RCV Id: RCV001995029
dbSNP Id: rs767090801

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45504416G>T , CM000683.2:g.45504416G>T GRCh38
NC_000021.8:g.46924330G>T , CM000683.1:g.46924330G>T GRCh37
NC_000021.7:g.45748758G>T NCBI36
NG_011903.1:g.104234G>T
NG_028278.2:g.63728C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000355480.10:c.3268G>T (COL18A1) ENSP00000347665.5:p.Gly1090Trp
ENST00000651438.1:c.2728G>T (COL18A1) MANE Select ENSP00000498485.1:p.Gly910Trp
ENST00000342220.9:c.769G>T (COL18A1) ENSP00000339118.5:p.Gly257Trp
ENST00000355480.9:c.3268G>T (COL18A1) ENSP00000347665.5:p.Gly1090Trp
ENST00000359759.8:c.3973G>T (COL18A1) ENSP00000352798.4:p.Gly1325Trp
ENST00000400337.6:c.2728G>T (COL18A1) ENSP00000383191.2:p.Gly910Trp
ENST00000417954.5:c.498-5804C>A (SLC19A1)
ENST00000567670.5:c.1294-5804C>A (SLC19A1) ENSP00000457278.1:n.1294-5804C>A
NM_030582.3:c.3268G>T (COL18A1) NP_085059.2:p.Gly1090Trp
NM_130444.2:c.3973G>T (COL18A1) NP_569711.2:p.Gly1325Trp
NM_130445.3:c.2728G>T (COL18A1) NP_569712.2:p.Gly910Trp
XM_011529707.1:c.1585-1447C>A (SLC19A1) XP_011528009.1:n.1585-1447C>A
XM_017028445.2:c.1585-1447C>A (SLC19A1) XP_016883934.1:n.1585-1447C>A
NM_030582.4:c.3268G>T (COL18A1) NP_085059.2:p.Gly1090Trp
NM_130444.3:c.3973G>T (COL18A1) NP_569711.2:p.Gly1325Trp
NM_130445.4:c.2728G>T (COL18A1) NP_569712.2:p.Gly910Trp
NM_001379500.1:c.2728G>T (COL18A1) MANE Select NP_001366429.1:p.Gly910Trp