Canonical Allele Identifier: CA2580098853

Gene: COL18A1 SLC19A1

Linked Data

• ClinVar Variation Id: 2088270
• ClinVar RCV Id: RCV003011556

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45505192_45505252del , CM000683.2:g.45505192_45505252del	GRCh38
NC_000021.8:g.46925106_46925166del , CM000683.1:g.46925106_46925166del	GRCh37
NC_000021.7:g.45749534_45749594del	NCBI36
NG_011903.1:g.105001_105061del
NG_028278.2:g.62896_62956del

Transcript Alleles

HGVS	Amino-acid change
ENST00000355480.10:c.3467_3527del (COL18A1)	ENSP00000347665.5:p.Pro1156LeufsTer?
ENST00000651438.1:c.2927_2987del (COL18A1) MANE Select	ENSP00000498485.1:p.Pro976LeufsTer?
ENST00000342220.9:c.968_1028del (COL18A1)	ENSP00000339118.5:p.Pro323LeufsTer?
ENST00000355480.9:c.3467_3527del (COL18A1)	ENSP00000347665.5:p.Pro1156LeufsTer?
ENST00000359759.8:c.4172_4232del (COL18A1)	ENSP00000352798.4:p.Pro1391LeufsTer?
ENST00000400337.6:c.2927_2987del (COL18A1)	ENSP00000383191.2:p.Pro976LeufsTer?
ENST00000417954.5:c.498-6636_498-6576del (SLC19A1)
ENST00000567670.5:c.1294-6636_1294-6576del (SLC19A1)	ENSP00000457278.1:n.1294-6636_1294-6576de...
NM_030582.3:c.3458_3518del (COL18A1)	NP_085059.2:p.Pro1153LeufsTer?
NM_130444.2:c.4163_4223del (COL18A1)	NP_569711.2:p.Pro1388LeufsTer?
NM_130445.3:c.2918_2978del (COL18A1)	NP_569712.2:p.Pro973LeufsTer?
XM_011529707.1:c.1585-2279_1585-2219del (SLC19A1)	XP_011528009.1:n.1585-2279_1585-2219del
XM_017028445.2:c.1585-2279_1585-2219del (SLC19A1)	XP_016883934.1:n.1585-2279_1585-2219del
NM_030582.4:c.3458_3518del (COL18A1)	NP_085059.2:p.Pro1153LeufsTer?
NM_130444.3:c.4163_4223del (COL18A1)	NP_569711.2:p.Pro1388LeufsTer?
NM_130445.4:c.2918_2978del (COL18A1)	NP_569712.2:p.Pro973LeufsTer?
NM_001379500.1:c.2927_2987del (COL18A1) MANE Select	NP_001366429.1:p.Pro976LeufsTer?