Canonical Allele Identifier: CA410499003

Gene: COL18A1 SLC19A1

Linked Data

• MyVariant Identifiers: chr21:g.46923936T>G (hg19) ; chr21:g.45504022T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45504022T>G , CM000683.2:g.45504022T>G	GRCh38
NC_000021.8:g.46923936T>G , CM000683.1:g.46923936T>G	GRCh37
NC_000021.7:g.45748364T>G	NCBI36
NG_011903.1:g.103840T>G
NG_028278.2:g.64122A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355480.10:c.3235T>G (COL18A1)	ENSP00000347665.5:p.Phe1079Val
ENST00000651438.1:c.2695T>G (COL18A1) MANE Select	ENSP00000498485.1:p.Phe899Val
ENST00000342220.9:c.736T>G (COL18A1)	ENSP00000339118.5:p.Phe246Val
ENST00000355480.9:c.3235T>G (COL18A1)	ENSP00000347665.5:p.Phe1079Val
ENST00000359759.8:c.3940T>G (COL18A1)	ENSP00000352798.4:p.Phe1314Val
ENST00000400337.6:c.2695T>G (COL18A1)	ENSP00000383191.2:p.Phe899Val
ENST00000417954.5:c.498-5410A>C (SLC19A1)
ENST00000461785.1:n.100A>C (SLC19A1)
ENST00000567670.5:c.1294-5410A>C (SLC19A1)	ENSP00000457278.1:n.1294-5410A>C
NM_030582.3:c.3235T>G (COL18A1)	NP_085059.2:p.Phe1079Val
NM_130444.2:c.3940T>G (COL18A1)	NP_569711.2:p.Phe1314Val
NM_130445.3:c.2695T>G (COL18A1)	NP_569712.2:p.Phe899Val
XM_011529707.1:c.1585-1053A>C (SLC19A1)	XP_011528009.1:n.1585-1053A>C
XM_017028445.2:c.1585-1053A>C (SLC19A1)	XP_016883934.1:n.1585-1053A>C
NM_030582.4:c.3235T>G (COL18A1)	NP_085059.2:p.Phe1079Val
NM_130444.3:c.3940T>G (COL18A1)	NP_569711.2:p.Phe1314Val
NM_130445.4:c.2695T>G (COL18A1)	NP_569712.2:p.Phe899Val
NM_001379500.1:c.2695T>G (COL18A1) MANE Select	NP_001366429.1:p.Phe899Val