Canonical Allele Identifier: CA2577627023

Gene: COL18A1 SLC19A1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45504513_45504522del , CM000683.2:g.45504513_45504522del	GRCh38
NC_000021.8:g.46924427_46924436del , CM000683.1:g.46924427_46924436del	GRCh37
NC_000021.7:g.45748855_45748864del	NCBI36
NG_028278.2:g.63623_63632del

Transcript Alleles

HGVS	Amino-acid change
ENST00000355480.10:c.3365_3374del (COL18A1)	ENSP00000347665.5:p.Gly1122AlafsTer?
ENST00000651438.1:c.2825_2834del (COL18A1) MANE Select	ENSP00000498485.1:p.Gly942AlafsTer?
ENST00000342220.9:c.866_875del (COL18A1)	ENSP00000339118.5:p.Gly289AlafsTer?
ENST00000355480.9:c.3365_3374del (COL18A1)	ENSP00000347665.5:p.Gly1122AlafsTer?
ENST00000359759.8:c.4070_4079del (COL18A1)	ENSP00000352798.4:p.Gly1357AlafsTer?
ENST00000400337.6:c.2825_2834del (COL18A1)	ENSP00000383191.2:p.Gly942AlafsTer?
ENST00000417954.5:c.498-5909_498-5900del (SLC19A1)
ENST00000567670.5:c.1294-5909_1294-5900del (SLC19A1)	ENSP00000457278.1:n.1294-5909_1294-5900de...
NM_030582.3:c.3365_3374del (COL18A1)	NP_085059.2:p.Gly1122AlafsTer?
NM_130444.2:c.4070_4079del (COL18A1)	NP_569711.2:p.Gly1357AlafsTer?
NM_130445.3:c.2825_2834del (COL18A1)	NP_569712.2:p.Gly942AlafsTer?
XM_011529707.1:c.1585-1552_1585-1543del (SLC19A1)	XP_011528009.1:n.1585-1552_1585-1543del
XM_017028445.2:c.1585-1552_1585-1543del (SLC19A1)	XP_016883934.1:n.1585-1552_1585-1543del
NM_030582.4:c.3365_3374del (COL18A1)	NP_085059.2:p.Gly1122AlafsTer?
NM_130444.3:c.4070_4079del (COL18A1)	NP_569711.2:p.Gly1357AlafsTer?
NM_130445.4:c.2825_2834del (COL18A1)	NP_569712.2:p.Gly942AlafsTer?
NM_001379500.1:c.2825_2834del (COL18A1) MANE Select	NP_001366429.1:p.Gly942AlafsTer?