Canonical Allele Identifier: CA10067548
Gene: COL18A1 HGNC NCBI
SLC19A1 HGNC NCBI

Linked Data

dbSNP Id: rs760921086

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45505173C>A , CM000683.2:g.45505173C>A GRCh38
NC_000021.8:g.46925087C>A , CM000683.1:g.46925087C>A GRCh37
NC_000021.7:g.45749515C>A NCBI36
NG_011903.1:g.104982C>A
NG_028278.2:g.62971G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355480.10:c.3448C>A (COL18A1) ENSP00000347665.5:p.Pro1150Thr
ENST00000651438.1:c.2908C>A (COL18A1) MANE Select ENSP00000498485.1:p.Pro970Thr
ENST00000342220.9:c.949C>A (COL18A1) ENSP00000339118.5:p.Pro317Thr
ENST00000355480.9:c.3448C>A (COL18A1) ENSP00000347665.5:p.Pro1150Thr
ENST00000359759.8:c.4153C>A (COL18A1) ENSP00000352798.4:p.Pro1385Thr
ENST00000400337.6:c.2908C>A (COL18A1) ENSP00000383191.2:p.Pro970Thr
ENST00000417954.5:c.498-6561G>T (SLC19A1)
ENST00000567670.5:c.1294-6561G>T (SLC19A1) ENSP00000457278.1:n.1294-6561G>T
NM_030582.3:c.3439C>A (COL18A1) NP_085059.2:p.Pro1147Thr
NM_130444.2:c.4144C>A (COL18A1) NP_569711.2:p.Pro1382Thr
NM_130445.3:c.2899C>A (COL18A1) NP_569712.2:p.Pro967Thr
XM_011529707.1:c.1585-2204G>T (SLC19A1) XP_011528009.1:n.1585-2204G>T
XM_017028445.2:c.1585-2204G>T (SLC19A1) XP_016883934.1:n.1585-2204G>T
NM_030582.4:c.3439C>A (COL18A1) NP_085059.2:p.Pro1147Thr
NM_130444.3:c.4144C>A (COL18A1) NP_569711.2:p.Pro1382Thr
NM_130445.4:c.2899C>A (COL18A1) NP_569712.2:p.Pro967Thr
NM_001379500.1:c.2908C>A (COL18A1) MANE Select NP_001366429.1:p.Pro970Thr