Canonical Allele Identifier: CA2392196254

Gene: COL18A1 SLC19A1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45511752C= , CM000683.2:g.45511752C=	GRCh38
NC_000021.8:g.46931666C= , CM000683.1:g.46931666C=	GRCh37
NC_000021.7:g.45756094C=	NCBI36
NG_011903.1:g.111561C=
NG_028278.2:g.56392G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355480.10:c.4350-436C= (COL18A1)	ENSP00000347665.5:n.4350-436C=
ENST00000651438.1:c.3810-436C= (COL18A1) MANE Select	ENSP00000498485.1:n.3810-436C=
ENST00000342220.9:c.1854-436C= (COL18A1)	ENSP00000339118.5:n.1854-436C=
ENST00000355480.9:c.4350-436C= (COL18A1)	ENSP00000347665.5:n.4350-436C=
ENST00000359759.8:c.5055-436C= (COL18A1)	ENSP00000352798.4:n.5055-436C=
ENST00000400337.6:c.3810-436C= (COL18A1)	ENSP00000383191.2:n.3810-436C=
ENST00000417954.5:c.498-13140G= (SLC19A1)
ENST00000423214.1:c.764-436C= (COL18A1)
ENST00000473212.1:n.2136-436C= (COL18A1)
ENST00000567670.5:c.1294-13140G= (SLC19A1)	ENSP00000457278.1:n.1294-13140G=
NM_030582.3:c.4341-436C= (COL18A1)	NP_085059.2:n.4341-436C=
NM_130444.2:c.5046-436C= (COL18A1)	NP_569711.2:n.5046-436C=
NM_130445.3:c.3801-436C= (COL18A1)	NP_569712.2:n.3801-436C=
XM_011529707.1:c.1585-8783G= (SLC19A1)	XP_011528009.1:n.1585-8783G=
XM_017028445.2:c.1585-8783G= (SLC19A1)	XP_016883934.1:n.1585-8783G=
NM_030582.4:c.4341-436C= (COL18A1)	NP_085059.2:n.4341-436C=
NM_130444.3:c.5046-436C= (COL18A1)	NP_569711.2:n.5046-436C=
NM_130445.4:c.3801-436C= (COL18A1)	NP_569712.2:n.3801-436C=
NM_001379500.1:c.3810-436C= (COL18A1) MANE Select	NP_001366429.1:n.3810-436C=