Canonical Allele Identifier: CA2392190729

Gene: COL18A1 SLC19A1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45504508_45504512delinsCCCCG , CM000683.2:g.45504508_45504512delinsCCCCG	GRCh38
NC_000021.8:g.46924422_46924426delinsCCCCG , CM000683.1:g.46924422_46924426delinsCCCCG	GRCh37
NC_000021.7:g.45748850_45748854delinsCCCCG	NCBI36
NG_028278.2:g.63632_63636delinsCGGGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000355480.10:c.3360_3364delinsCCCCG (COL18A1)	ENSP00000347665.5:p.Pro1120=
ENST00000651438.1:c.2820_2824delinsCCCCG (COL18A1) MANE Select	ENSP00000498485.1:p.Pro940=
ENST00000342220.9:c.861_865delinsCCCCG (COL18A1)	ENSP00000339118.5:p.Pro287=
ENST00000355480.9:c.3360_3364delinsCCCCG (COL18A1)	ENSP00000347665.5:p.Pro1120=
ENST00000359759.8:c.4065_4069delinsCCCCG (COL18A1)	ENSP00000352798.4:p.Pro1355=
ENST00000400337.6:c.2820_2824delinsCCCCG (COL18A1)	ENSP00000383191.2:p.Pro940=
ENST00000417954.5:c.498-5900_498-5896delinsCGGGG (SLC19A1)
ENST00000567670.5:c.1294-5900_1294-5896delinsCGGGG (SLC19A1)	ENSP00000457278.1:n.1294-5900_1294-5896de...
NM_030582.3:c.3360_3364delinsCCCCG (COL18A1)	NP_085059.2:p.Pro1120=
NM_130444.2:c.4065_4069delinsCCCCG (COL18A1)	NP_569711.2:p.Pro1355=
NM_130445.3:c.2820_2824delinsCCCCG (COL18A1)	NP_569712.2:p.Pro940=
XM_011529707.1:c.1585-1543_1585-1539delinsCGGGG (SLC19A1)	XP_011528009.1:n.1585-1543_1585-1539delin...
XM_017028445.2:c.1585-1543_1585-1539delinsCGGGG (SLC19A1)	XP_016883934.1:n.1585-1543_1585-1539delin...
NM_030582.4:c.3360_3364delinsCCCCG (COL18A1)	NP_085059.2:p.Pro1120=
NM_130444.3:c.4065_4069delinsCCCCG (COL18A1)	NP_569711.2:p.Pro1355=
NM_130445.4:c.2820_2824delinsCCCCG (COL18A1)	NP_569712.2:p.Pro940=
NM_001379500.1:c.2820_2824delinsCCCCG (COL18A1) MANE Select	NP_001366429.1:p.Pro940=