Canonical Allele Identifier: CA512687222

Gene: COL18A1 SLC19A1

Linked Data

• gnomAD v4: 21-45505160-C-G
• MyVariant Identifiers: chr21:g.46925074C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45505160C>G , CM000683.2:g.45505160C>G	GRCh38
NC_000021.8:g.46925074C>G , CM000683.1:g.46925074C>G	GRCh37
NC_000021.7:g.45749502C>G	NCBI36
NG_011903.1:g.104969C>G
NG_028278.2:g.62984G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355480.10:c.3435C>G (COL18A1)	ENSP00000347665.5:p.Gly1145=
ENST00000651438.1:c.2895C>G (COL18A1) MANE Select	ENSP00000498485.1:p.Gly965=
ENST00000342220.9:c.936C>G (COL18A1)	ENSP00000339118.5:p.Gly312=
ENST00000355480.9:c.3435C>G (COL18A1)	ENSP00000347665.5:p.Gly1145=
ENST00000359759.8:c.4140C>G (COL18A1)	ENSP00000352798.4:p.Gly1380=
ENST00000400337.6:c.2895C>G (COL18A1)	ENSP00000383191.2:p.Gly965=
ENST00000417954.5:c.498-6548G>C (SLC19A1)
ENST00000567670.5:c.1294-6548G>C (SLC19A1)	ENSP00000457278.1:n.1294-6548G>C
NM_030582.3:c.3426C>G (COL18A1)	NP_085059.2:p.Gly1142=
NM_130444.2:c.4131C>G (COL18A1)	NP_569711.2:p.Gly1377=
NM_130445.3:c.2886C>G (COL18A1)	NP_569712.2:p.Gly962=
XM_011529707.1:c.1585-2191G>C (SLC19A1)	XP_011528009.1:n.1585-2191G>C
XM_017028445.2:c.1585-2191G>C (SLC19A1)	XP_016883934.1:n.1585-2191G>C
NM_030582.4:c.3426C>G (COL18A1)	NP_085059.2:p.Gly1142=
NM_130444.3:c.4131C>G (COL18A1)	NP_569711.2:p.Gly1377=
NM_130445.4:c.2886C>G (COL18A1)	NP_569712.2:p.Gly962=
NM_001379500.1:c.2895C>G (COL18A1) MANE Select	NP_001366429.1:p.Gly965=