Canonical Allele Identifier: CA2838854324

Gene: COL18A1 SLC19A1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45504142C>T , CM000683.2:g.45504142C>T	GRCh38
NC_000021.8:g.46924056C>T , CM000683.1:g.46924056C>T	GRCh37
NC_000021.7:g.45748484C>T	NCBI36
NG_011903.1:g.103960C>T
NG_028278.2:g.64002G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355480.10:c.3267+88C>T (COL18A1)	ENSP00000347665.5:n.3267+88C>T
ENST00000651438.1:c.2727+88C>T (COL18A1) MANE Select	ENSP00000498485.1:n.2727+88C>T
ENST00000342220.9:c.768+88C>T (COL18A1)	ENSP00000339118.5:n.768+88C>T
ENST00000355480.9:c.3267+88C>T (COL18A1)	ENSP00000347665.5:n.3267+88C>T
ENST00000359759.8:c.3972+88C>T (COL18A1)	ENSP00000352798.4:n.3972+88C>T
ENST00000400337.6:c.2727+88C>T (COL18A1)	ENSP00000383191.2:n.2727+88C>T
ENST00000417954.5:c.498-5530G>A (SLC19A1)
ENST00000567670.5:c.1294-5530G>A (SLC19A1)	ENSP00000457278.1:n.1294-5530G>A
NM_030582.3:c.3267+88C>T (COL18A1)	NP_085059.2:n.3267+88C>T
NM_130444.2:c.3972+88C>T (COL18A1)	NP_569711.2:n.3972+88C>T
NM_130445.3:c.2727+88C>T (COL18A1)	NP_569712.2:n.2727+88C>T
XM_011529707.1:c.1585-1173G>A (SLC19A1)	XP_011528009.1:n.1585-1173G>A
XM_017028445.2:c.1585-1173G>A (SLC19A1)	XP_016883934.1:n.1585-1173G>A
NM_030582.4:c.3267+88C>T (COL18A1)	NP_085059.2:n.3267+88C>T
NM_130444.3:c.3972+88C>T (COL18A1)	NP_569711.2:n.3972+88C>T
NM_130445.4:c.2727+88C>T (COL18A1)	NP_569712.2:n.2727+88C>T
NM_001379500.1:c.2727+88C>T (COL18A1) MANE Select	NP_001366429.1:n.2727+88C>T