Canonical Allele Identifier: CA2542280939

Gene: COL18A1 SLC19A1

Linked Data

• ClinVar Variation Id: 2805804
• ClinVar RCV Id: RCV003676959
• gnomAD v4: 21-45504574-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45504574C>T , CM000683.2:g.45504574C>T	GRCh38
NC_000021.8:g.46924488C>T , CM000683.1:g.46924488C>T	GRCh37
NC_000021.7:g.45748916C>T	NCBI36
NG_011903.1:g.104383C>T
NG_028278.2:g.63570G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355480.10:c.3408+18C>T (COL18A1)	ENSP00000347665.5:n.3408+18C>T
ENST00000651438.1:c.2868+18C>T (COL18A1) MANE Select	ENSP00000498485.1:n.2868+18C>T
ENST00000342220.9:c.909+18C>T (COL18A1)	ENSP00000339118.5:n.909+18C>T
ENST00000355480.9:c.3408+18C>T (COL18A1)	ENSP00000347665.5:n.3408+18C>T
ENST00000359759.8:c.4113+18C>T (COL18A1)	ENSP00000352798.4:n.4113+18C>T
ENST00000400337.6:c.2868+18C>T (COL18A1)	ENSP00000383191.2:n.2868+18C>T
ENST00000417954.5:c.498-5962G>A (SLC19A1)
ENST00000567670.5:c.1294-5962G>A (SLC19A1)	ENSP00000457278.1:n.1294-5962G>A
NM_030582.3:c.3399+18C>T (COL18A1)	NP_085059.2:n.3399+18C>T
NM_130444.2:c.4104+18C>T (COL18A1)	NP_569711.2:n.4104+18C>T
NM_130445.3:c.2859+18C>T (COL18A1)	NP_569712.2:n.2859+18C>T
XM_011529707.1:c.1585-1605G>A (SLC19A1)	XP_011528009.1:n.1585-1605G>A
XM_017028445.2:c.1585-1605G>A (SLC19A1)	XP_016883934.1:n.1585-1605G>A
NM_030582.4:c.3399+18C>T (COL18A1)	NP_085059.2:n.3399+18C>T
NM_130444.3:c.4104+18C>T (COL18A1)	NP_569711.2:n.4104+18C>T
NM_130445.4:c.2859+18C>T (COL18A1)	NP_569712.2:n.2859+18C>T
NM_001379500.1:c.2868+18C>T (COL18A1) MANE Select	NP_001366429.1:n.2868+18C>T