Canonical Allele Identifier: CA2392190835

Gene: COL18A1 SLC19A1

Linked Data

• dbSNP Id: rs2037074712

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45504623T>C , CM000683.2:g.45504623T>C	GRCh38
NC_000021.8:g.46924537T>C , CM000683.1:g.46924537T>C	GRCh37
NC_000021.7:g.45748965T>C	NCBI36
NG_011903.1:g.104432T>C
NG_028278.2:g.63521A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355480.10:c.3408+67T>C (COL18A1)	ENSP00000347665.5:n.3408+67T>C
ENST00000651438.1:c.2868+67T>C (COL18A1) MANE Select	ENSP00000498485.1:n.2868+67T>C
ENST00000342220.9:c.909+67T>C (COL18A1)	ENSP00000339118.5:n.909+67T>C
ENST00000355480.9:c.3408+67T>C (COL18A1)	ENSP00000347665.5:n.3408+67T>C
ENST00000359759.8:c.4113+67T>C (COL18A1)	ENSP00000352798.4:n.4113+67T>C
ENST00000400337.6:c.2868+67T>C (COL18A1)	ENSP00000383191.2:n.2868+67T>C
ENST00000417954.5:c.498-6011A>G (SLC19A1)
ENST00000567670.5:c.1294-6011A>G (SLC19A1)	ENSP00000457278.1:n.1294-6011A>G
NM_030582.3:c.3399+67T>C (COL18A1)	NP_085059.2:n.3399+67T>C
NM_130444.2:c.4104+67T>C (COL18A1)	NP_569711.2:n.4104+67T>C
NM_130445.3:c.2859+67T>C (COL18A1)	NP_569712.2:n.2859+67T>C
XM_011529707.1:c.1585-1654A>G (SLC19A1)	XP_011528009.1:n.1585-1654A>G
XM_017028445.2:c.1585-1654A>G (SLC19A1)	XP_016883934.1:n.1585-1654A>G
NM_030582.4:c.3399+67T>C (COL18A1)	NP_085059.2:n.3399+67T>C
NM_130444.3:c.4104+67T>C (COL18A1)	NP_569711.2:n.4104+67T>C
NM_130445.4:c.2859+67T>C (COL18A1)	NP_569712.2:n.2859+67T>C
NM_001379500.1:c.2868+67T>C (COL18A1) MANE Select	NP_001366429.1:n.2868+67T>C