Canonical Allele Identifier: CA321921087

Gene: COL18A1 SLC19A1

Linked Data

• dbSNP Id: rs926391472
• gnomAD v2: 21-46923719-AAAAAT-A
• gnomAD v3: 21-45503805-AAAAAT-A
• gnomAD v4: 21-45503805-AAAAAT-A
• MyVariant Identifiers: chr21:g.46923720_46923724del (hg19) ; chr21:g.45503806_45503810del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45503815_45503819del , CM000683.2:g.45503815_45503819del	GRCh38
NC_000021.8:g.46923729_46923733del , CM000683.1:g.46923729_46923733del	GRCh37
NC_000021.7:g.45748157_45748161del	NCBI36
NG_011903.1:g.103633_103637del
NG_028278.2:g.64334_64338del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355480.10:c.3224-196_3224-192del (COL18A1)	ENSP00000347665.5:n.3224-196_3224-192del
ENST00000651438.1:c.2684-196_2684-192del (COL18A1) MANE Select	ENSP00000498485.1:n.2684-196_2684-192del
ENST00000342220.9:c.725-196_725-192del (COL18A1)	ENSP00000339118.5:n.725-196_725-192del
ENST00000355480.9:c.3224-196_3224-192del (COL18A1)	ENSP00000347665.5:n.3224-196_3224-192del
ENST00000359759.8:c.3929-196_3929-192del (COL18A1)	ENSP00000352798.4:n.3929-196_3929-192del
ENST00000400337.6:c.2684-196_2684-192del (COL18A1)	ENSP00000383191.2:n.2684-196_2684-192del
ENST00000417954.5:c.498-5198_498-5194del (SLC19A1)
ENST00000461785.1:n.189+123_189+127del (SLC19A1)
ENST00000567670.5:c.1294-5198_1294-5194del (SLC19A1)	ENSP00000457278.1:n.1294-5198_1294-5194del
NM_030582.3:c.3224-196_3224-192del (COL18A1)	NP_085059.2:n.3224-196_3224-192del
NM_130444.2:c.3929-196_3929-192del (COL18A1)	NP_569711.2:n.3929-196_3929-192del
NM_130445.3:c.2684-196_2684-192del (COL18A1)	NP_569712.2:n.2684-196_2684-192del
XM_011529707.1:c.1585-841_1585-837del (SLC19A1)	XP_011528009.1:n.1585-841_1585-837del
XM_017028445.2:c.1585-841_1585-837del (SLC19A1)	XP_016883934.1:n.1585-841_1585-837del
NM_030582.4:c.3224-196_3224-192del (COL18A1)	NP_085059.2:n.3224-196_3224-192del
NM_130444.3:c.3929-196_3929-192del (COL18A1)	NP_569711.2:n.3929-196_3929-192del
NM_130445.4:c.2684-196_2684-192del (COL18A1)	NP_569712.2:n.2684-196_2684-192del
NM_001379500.1:c.2684-196_2684-192del (COL18A1) MANE Select	NP_001366429.1:n.2684-196_2684-192del