Canonical Allele Identifier: CA410499442

Gene: COL18A1 SLC19A1

Linked Data

• MyVariant Identifiers: chr21:g.46925082G>T (hg19) ; chr21:g.45505168G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45505168G>T , CM000683.2:g.45505168G>T	GRCh38
NC_000021.8:g.46925082G>T , CM000683.1:g.46925082G>T	GRCh37
NC_000021.7:g.45749510G>T	NCBI36
NG_011903.1:g.104977G>T
NG_028278.2:g.62976C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355480.10:c.3443G>T (COL18A1)	ENSP00000347665.5:p.Gly1148Val
ENST00000651438.1:c.2903G>T (COL18A1) MANE Select	ENSP00000498485.1:p.Gly968Val
ENST00000342220.9:c.944G>T (COL18A1)	ENSP00000339118.5:p.Gly315Val
ENST00000355480.9:c.3443G>T (COL18A1)	ENSP00000347665.5:p.Gly1148Val
ENST00000359759.8:c.4148G>T (COL18A1)	ENSP00000352798.4:p.Gly1383Val
ENST00000400337.6:c.2903G>T (COL18A1)	ENSP00000383191.2:p.Gly968Val
ENST00000417954.5:c.498-6556C>A (SLC19A1)
ENST00000567670.5:c.1294-6556C>A (SLC19A1)	ENSP00000457278.1:n.1294-6556C>A
NM_030582.3:c.3434G>T (COL18A1)	NP_085059.2:p.Gly1145Val
NM_130444.2:c.4139G>T (COL18A1)	NP_569711.2:p.Gly1380Val
NM_130445.3:c.2894G>T (COL18A1)	NP_569712.2:p.Gly965Val
XM_011529707.1:c.1585-2199C>A (SLC19A1)	XP_011528009.1:n.1585-2199C>A
XM_017028445.2:c.1585-2199C>A (SLC19A1)	XP_016883934.1:n.1585-2199C>A
NM_030582.4:c.3434G>T (COL18A1)	NP_085059.2:p.Gly1145Val
NM_130444.3:c.4139G>T (COL18A1)	NP_569711.2:p.Gly1380Val
NM_130445.4:c.2894G>T (COL18A1)	NP_569712.2:p.Gly965Val
NM_001379500.1:c.2903G>T (COL18A1) MANE Select	NP_001366429.1:p.Gly968Val