Canonical Allele Identifier: CA2392196190

Gene: COL18A1 SLC19A1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45511661T= , CM000683.2:g.45511661T=	GRCh38
NC_000021.8:g.46931575T= , CM000683.1:g.46931575T=	GRCh37
NC_000021.7:g.45756003T=	NCBI36
NG_011903.1:g.111470T=
NG_028278.2:g.56483A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355480.10:c.4349+435T= (COL18A1)	ENSP00000347665.5:n.4349+435T=
ENST00000651438.1:c.3809+435T= (COL18A1) MANE Select	ENSP00000498485.1:n.3809+435T=
ENST00000342220.9:c.1853+435T= (COL18A1)	ENSP00000339118.5:n.1853+435T=
ENST00000355480.9:c.4349+435T= (COL18A1)	ENSP00000347665.5:n.4349+435T=
ENST00000359759.8:c.5054+435T= (COL18A1)	ENSP00000352798.4:n.5054+435T=
ENST00000400337.6:c.3809+435T= (COL18A1)	ENSP00000383191.2:n.3809+435T=
ENST00000417954.5:c.498-13049A= (SLC19A1)
ENST00000423214.1:c.763+435T= (COL18A1)
ENST00000473212.1:n.2135+435T= (COL18A1)
ENST00000567670.5:c.1294-13049A= (SLC19A1)	ENSP00000457278.1:n.1294-13049A=
NM_030582.3:c.4340+435T= (COL18A1)	NP_085059.2:n.4340+435T=
NM_130444.2:c.5045+435T= (COL18A1)	NP_569711.2:n.5045+435T=
NM_130445.3:c.3800+435T= (COL18A1)	NP_569712.2:n.3800+435T=
XM_011529707.1:c.1585-8692A= (SLC19A1)	XP_011528009.1:n.1585-8692A=
XM_017028445.2:c.1585-8692A= (SLC19A1)	XP_016883934.1:n.1585-8692A=
NM_030582.4:c.4340+435T= (COL18A1)	NP_085059.2:n.4340+435T=
NM_130444.3:c.5045+435T= (COL18A1)	NP_569711.2:n.5045+435T=
NM_130445.4:c.3800+435T= (COL18A1)	NP_569712.2:n.3800+435T=
NM_001379500.1:c.3809+435T= (COL18A1) MANE Select	NP_001366429.1:n.3809+435T=