Canonical Allele Identifier: CA321926979

Gene: COL18A1 SLC19A1

Linked Data

• dbSNP Id: rs1031399649
• gnomAD v2: 21-46931589-G-A
• gnomAD v3: 21-45511675-G-A
• gnomAD v4: 21-45511675-G-A
• MyVariant Identifiers: chr21:g.46931589G>A (hg19) ; chr21:g.45511675G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45511675G>A , CM000683.2:g.45511675G>A	GRCh38
NC_000021.8:g.46931589G>A , CM000683.1:g.46931589G>A	GRCh37
NC_000021.7:g.45756017G>A	NCBI36
NG_011903.1:g.111484G>A
NG_028278.2:g.56469C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000355480.10:c.4349+449G>A (COL18A1)	ENSP00000347665.5:n.4349+449G>A
ENST00000651438.1:c.3809+449G>A (COL18A1) MANE Select	ENSP00000498485.1:n.3809+449G>A
ENST00000342220.9:c.1853+449G>A (COL18A1)	ENSP00000339118.5:n.1853+449G>A
ENST00000355480.9:c.4349+449G>A (COL18A1)	ENSP00000347665.5:n.4349+449G>A
ENST00000359759.8:c.5054+449G>A (COL18A1)	ENSP00000352798.4:n.5054+449G>A
ENST00000400337.6:c.3809+449G>A (COL18A1)	ENSP00000383191.2:n.3809+449G>A
ENST00000417954.5:c.498-13063C>T (SLC19A1)
ENST00000423214.1:c.763+449G>A (COL18A1)
ENST00000473212.1:n.2135+449G>A (COL18A1)
ENST00000567670.5:c.1294-13063C>T (SLC19A1)	ENSP00000457278.1:n.1294-13063C>T
NM_030582.3:c.4340+449G>A (COL18A1)	NP_085059.2:n.4340+449G>A
NM_130444.2:c.5045+449G>A (COL18A1)	NP_569711.2:n.5045+449G>A
NM_130445.3:c.3800+449G>A (COL18A1)	NP_569712.2:n.3800+449G>A
XM_011529707.1:c.1585-8706C>T (SLC19A1)	XP_011528009.1:n.1585-8706C>T
XM_017028445.2:c.1585-8706C>T (SLC19A1)	XP_016883934.1:n.1585-8706C>T
NM_030582.4:c.4340+449G>A (COL18A1)	NP_085059.2:n.4340+449G>A
NM_130444.3:c.5045+449G>A (COL18A1)	NP_569711.2:n.5045+449G>A
NM_130445.4:c.3800+449G>A (COL18A1)	NP_569712.2:n.3800+449G>A
NM_001379500.1:c.3809+449G>A (COL18A1) MANE Select	NP_001366429.1:n.3809+449G>A