Canonical Allele Identifier: CA2507755690

Gene: COL18A1 SLC19A1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45510952_45511015del , CM000683.2:g.45510952_45511015del	GRCh38
NC_000021.8:g.46930866_46930929del , CM000683.1:g.46930866_46930929del	GRCh37
NC_000021.7:g.45755294_45755357del	NCBI36
NG_011903.1:g.110761_110824del
NG_028278.2:g.57135_57198del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355480.10:c.4234-159_4234-96del (COL18A1)	ENSP00000347665.5:n.4234-159_4234-96del
ENST00000651438.1:c.3694-159_3694-96del (COL18A1) MANE Select	ENSP00000498485.1:n.3694-159_3694-96del
ENST00000342220.9:c.1738-159_1738-96del (COL18A1)	ENSP00000339118.5:n.1738-159_1738-96del
ENST00000355480.9:c.4234-159_4234-96del (COL18A1)	ENSP00000347665.5:n.4234-159_4234-96del
ENST00000359759.8:c.4939-159_4939-96del (COL18A1)	ENSP00000352798.4:n.4939-159_4939-96del
ENST00000400337.6:c.3694-159_3694-96del (COL18A1)	ENSP00000383191.2:n.3694-159_3694-96del
ENST00000417954.5:c.498-12397_498-12334del (SLC19A1)
ENST00000423214.1:c.648-159_648-96del (COL18A1)
ENST00000473212.1:n.2020-159_2020-96del (COL18A1)
ENST00000567670.5:c.1294-12397_1294-12334del (SLC19A1)	ENSP00000457278.1:n.1294-12397_1294-12334del
NM_030582.3:c.4225-159_4225-96del (COL18A1)	NP_085059.2:n.4225-159_4225-96del
NM_130444.2:c.4930-159_4930-96del (COL18A1)	NP_569711.2:n.4930-159_4930-96del
NM_130445.3:c.3685-159_3685-96del (COL18A1)	NP_569712.2:n.3685-159_3685-96del
XM_011529707.1:c.1585-8040_1585-7977del (SLC19A1)	XP_011528009.1:n.1585-8040_1585-7977del
XM_017028445.2:c.1585-8040_1585-7977del (SLC19A1)	XP_016883934.1:n.1585-8040_1585-7977del
NM_030582.4:c.4225-159_4225-96del (COL18A1)	NP_085059.2:n.4225-159_4225-96del
NM_130444.3:c.4930-159_4930-96del (COL18A1)	NP_569711.2:n.4930-159_4930-96del
NM_130445.4:c.3685-159_3685-96del (COL18A1)	NP_569712.2:n.3685-159_3685-96del
NM_001379500.1:c.3694-159_3694-96del (COL18A1) MANE Select	NP_001366429.1:n.3694-159_3694-96del