Canonical Allele Identifier: CA2392194569

Gene: COL18A1 SLC19A1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45509554C= , CM000683.2:g.45509554C=	GRCh38
NC_000021.8:g.46929468C= , CM000683.1:g.46929468C=	GRCh37
NC_000021.7:g.45753896C=	NCBI36
NG_011903.1:g.109363C=
NG_028278.2:g.58590G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001379500.1:c.3448C= (COL18A1) MANE Select	NP_001366429.1:p.Arg1150=
ENST00000651438.1:c.3448C= (COL18A1) MANE Select	ENSP00000498485.1:p.Arg1150=
NM_030582.3:c.3979C= (COL18A1)	NP_085059.2:p.Arg1327=
NM_030582.4:c.3979C= (COL18A1)	NP_085059.2:p.Arg1327=
NM_130444.2:c.4684C= (COL18A1)	NP_569711.2:p.Arg1562=
NM_130444.3:c.4684C= (COL18A1)	NP_569711.2:p.Arg1562=
NM_130445.3:c.3439C= (COL18A1)	NP_569712.2:p.Arg1147=
NM_130445.4:c.3439C= (COL18A1)	NP_569712.2:p.Arg1147=
ENST00000342220.9:c.1492C= (COL18A1)	ENSP00000339118.5:p.Arg498=
ENST00000355480.10:c.3988C= (COL18A1)	ENSP00000347665.5:p.Arg1330=
ENST00000355480.9:c.3988C= (COL18A1)	ENSP00000347665.5:p.Arg1330=
ENST00000359759.8:c.4693C= (COL18A1)	ENSP00000352798.4:p.Arg1565=
ENST00000400337.6:c.3448C= (COL18A1)	ENSP00000383191.2:p.Arg1150=
ENST00000417954.5:c.498-10942G= (SLC19A1)
ENST00000423214.1:c.402C= (COL18A1)
ENST00000473212.1:n.1774C= (COL18A1)
ENST00000567670.5:c.1294-10942G= (SLC19A1)	ENSP00000457278.1:n.1294-10942G=
XM_011529707.1:c.1585-6585G= (SLC19A1)	XP_011528009.1:n.1585-6585G=
XM_017028445.2:c.1585-6585G= (SLC19A1)	XP_016883934.1:n.1585-6585G=