Canonical Allele Identifier: CA512687715

Gene: COL18A1 SLC19A1

Linked Data

• MyVariant Identifiers: chr21:g.46931114C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45511200C>G , CM000683.2:g.45511200C>G	GRCh38
NC_000021.8:g.46931114C>G , CM000683.1:g.46931114C>G	GRCh37
NC_000021.7:g.45755542C>G	NCBI36
NG_011903.1:g.111009C>G
NG_028278.2:g.56944G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355480.10:c.4323C>G (COL18A1)	ENSP00000347665.5:p.Gly1441=
ENST00000651438.1:c.3783C>G (COL18A1) MANE Select	ENSP00000498485.1:p.Gly1261=
ENST00000342220.9:c.1827C>G (COL18A1)	ENSP00000339118.5:p.Gly609=
ENST00000355480.9:c.4323C>G (COL18A1)	ENSP00000347665.5:p.Gly1441=
ENST00000359759.8:c.5028C>G (COL18A1)	ENSP00000352798.4:p.Gly1676=
ENST00000400337.6:c.3783C>G (COL18A1)	ENSP00000383191.2:p.Gly1261=
ENST00000417954.5:c.498-12588G>C (SLC19A1)
ENST00000423214.1:c.737C>G (COL18A1)
ENST00000473212.1:n.2109C>G (COL18A1)
ENST00000567670.5:c.1294-12588G>C (SLC19A1)	ENSP00000457278.1:n.1294-12588G>C
NM_030582.3:c.4314C>G (COL18A1)	NP_085059.2:p.Gly1438=
NM_130444.2:c.5019C>G (COL18A1)	NP_569711.2:p.Gly1673=
NM_130445.3:c.3774C>G (COL18A1)	NP_569712.2:p.Gly1258=
XM_011529707.1:c.1585-8231G>C (SLC19A1)	XP_011528009.1:n.1585-8231G>C
XM_017028445.2:c.1585-8231G>C (SLC19A1)	XP_016883934.1:n.1585-8231G>C
NM_030582.4:c.4314C>G (COL18A1)	NP_085059.2:p.Gly1438=
NM_130444.3:c.5019C>G (COL18A1)	NP_569711.2:p.Gly1673=
NM_130445.4:c.3774C>G (COL18A1)	NP_569712.2:p.Gly1258=
NM_001379500.1:c.3783C>G (COL18A1) MANE Select	NP_001366429.1:p.Gly1261=