Canonical Allele Identifier: CA749787816

Gene: COL18A1 SLC19A1

Linked Data

• dbSNP Id: rs1204469850
• gnomAD v3: 21-45504703-TGG-T
• gnomAD v4: 21-45504703-TGG-T
• MyVariant Identifiers: chr21:g.46924618_46924619del (hg19) ; chr21:g.45504704_45504705del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45504706_45504707del , CM000683.2:g.45504706_45504707del	GRCh38
NC_000021.8:g.46924620_46924621del , CM000683.1:g.46924620_46924621del	GRCh37
NC_000021.7:g.45749048_45749049del	NCBI36
NG_011903.1:g.104515_104516del
NG_028278.2:g.63439_63440del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355480.10:c.3408+150_3408+151del (COL18A1)	ENSP00000347665.5:n.3408+150_3408+151del
ENST00000651438.1:c.2868+150_2868+151del (COL18A1) MANE Select	ENSP00000498485.1:n.2868+150_2868+151del
ENST00000342220.9:c.909+150_909+151del (COL18A1)	ENSP00000339118.5:n.909+150_909+151del
ENST00000355480.9:c.3408+150_3408+151del (COL18A1)	ENSP00000347665.5:n.3408+150_3408+151del
ENST00000359759.8:c.4113+150_4113+151del (COL18A1)	ENSP00000352798.4:n.4113+150_4113+151del
ENST00000400337.6:c.2868+150_2868+151del (COL18A1)	ENSP00000383191.2:n.2868+150_2868+151del
ENST00000417954.5:c.498-6093_498-6092del (SLC19A1)
ENST00000567670.5:c.1294-6093_1294-6092del (SLC19A1)	ENSP00000457278.1:n.1294-6093_1294-6092del
NM_030582.3:c.3399+150_3399+151del (COL18A1)	NP_085059.2:n.3399+150_3399+151del
NM_130444.2:c.4104+150_4104+151del (COL18A1)	NP_569711.2:n.4104+150_4104+151del
NM_130445.3:c.2859+150_2859+151del (COL18A1)	NP_569712.2:n.2859+150_2859+151del
XM_011529707.1:c.1585-1736_1585-1735del (SLC19A1)	XP_011528009.1:n.1585-1736_1585-1735del
XM_017028445.2:c.1585-1736_1585-1735del (SLC19A1)	XP_016883934.1:n.1585-1736_1585-1735del
NM_030582.4:c.3399+150_3399+151del (COL18A1)	NP_085059.2:n.3399+150_3399+151del
NM_130444.3:c.4104+150_4104+151del (COL18A1)	NP_569711.2:n.4104+150_4104+151del
NM_130445.4:c.2859+150_2859+151del (COL18A1)	NP_569712.2:n.2859+150_2859+151del
NM_001379500.1:c.2868+150_2868+151del (COL18A1) MANE Select	NP_001366429.1:n.2868+150_2868+151del