Canonical Allele Identifier: CA2654930597
Gene: COL18A1 HGNC NCBI
SLC19A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45510014T>A , CM000683.2:g.45510014T>A GRCh38
NC_000021.8:g.46929928T>A , CM000683.1:g.46929928T>A GRCh37
NC_000021.7:g.45754356T>A NCBI36
NG_011903.1:g.109823T>A
NG_028278.2:g.58130A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355480.10:c.4036-50T>A (COL18A1) ENSP00000347665.5:n.4036-50T>A
ENST00000651438.1:c.3496-50T>A (COL18A1) MANE Select ENSP00000498485.1:n.3496-50T>A
ENST00000342220.9:c.1540-50T>A (COL18A1) ENSP00000339118.5:n.1540-50T>A
ENST00000355480.9:c.4036-50T>A (COL18A1) ENSP00000347665.5:n.4036-50T>A
ENST00000359759.8:c.4741-50T>A (COL18A1) ENSP00000352798.4:n.4741-50T>A
ENST00000400337.6:c.3496-50T>A (COL18A1) ENSP00000383191.2:n.3496-50T>A
ENST00000417954.5:c.498-11402A>T (SLC19A1)
ENST00000423214.1:c.450-50T>A (COL18A1)
ENST00000473212.1:n.1822-50T>A (COL18A1)
ENST00000567670.5:c.1294-11402A>T (SLC19A1) ENSP00000457278.1:n.1294-11402A>T
NM_030582.3:c.4027-50T>A (COL18A1) NP_085059.2:n.4027-50T>A
NM_130444.2:c.4732-50T>A (COL18A1) NP_569711.2:n.4732-50T>A
NM_130445.3:c.3487-50T>A (COL18A1) NP_569712.2:n.3487-50T>A
XM_011529707.1:c.1585-7045A>T (SLC19A1) XP_011528009.1:n.1585-7045A>T
XM_017028445.2:c.1585-7045A>T (SLC19A1) XP_016883934.1:n.1585-7045A>T
NM_030582.4:c.4027-50T>A (COL18A1) NP_085059.2:n.4027-50T>A
NM_130444.3:c.4732-50T>A (COL18A1) NP_569711.2:n.4732-50T>A
NM_130445.4:c.3487-50T>A (COL18A1) NP_569712.2:n.3487-50T>A
NM_001379500.1:c.3496-50T>A (COL18A1) MANE Select NP_001366429.1:n.3496-50T>A