Canonical Allele Identifier: CA1022830520
Gene: COL18A1 HGNC NCBI
SLC19A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45510947_45511057del , CM000683.2:g.45510947_45511057del GRCh38
NC_000021.8:g.46930861_46930971del , CM000683.1:g.46930861_46930971del GRCh37
NC_000021.7:g.45755289_45755399del NCBI36
NG_011903.1:g.110756_110866del
NG_028278.2:g.57090_57200del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355480.10:c.4234-164_4234-54del (COL18A1) ENSP00000347665.5:n.4234-164_4234-54del
ENST00000651438.1:c.3694-164_3694-54del (COL18A1) MANE Select ENSP00000498485.1:n.3694-164_3694-54del
ENST00000342220.9:c.1738-164_1738-54del (COL18A1) ENSP00000339118.5:n.1738-164_1738-54del
ENST00000355480.9:c.4234-164_4234-54del (COL18A1) ENSP00000347665.5:n.4234-164_4234-54del
ENST00000359759.8:c.4939-164_4939-54del (COL18A1) ENSP00000352798.4:n.4939-164_4939-54del
ENST00000400337.6:c.3694-164_3694-54del (COL18A1) ENSP00000383191.2:n.3694-164_3694-54del
ENST00000417954.5:c.498-12442_498-12332del (SLC19A1)
ENST00000423214.1:c.648-164_648-54del (COL18A1)
ENST00000473212.1:n.2020-164_2020-54del (COL18A1)
ENST00000567670.5:c.1294-12442_1294-12332del (SLC19A1) ENSP00000457278.1:n.1294-12442_1294-12332del
NM_030582.3:c.4225-164_4225-54del (COL18A1) NP_085059.2:n.4225-164_4225-54del
NM_130444.2:c.4930-164_4930-54del (COL18A1) NP_569711.2:n.4930-164_4930-54del
NM_130445.3:c.3685-164_3685-54del (COL18A1) NP_569712.2:n.3685-164_3685-54del
XM_011529707.1:c.1585-8085_1585-7975del (SLC19A1) XP_011528009.1:n.1585-8085_1585-7975del
XM_017028445.2:c.1585-8085_1585-7975del (SLC19A1) XP_016883934.1:n.1585-8085_1585-7975del
NM_030582.4:c.4225-164_4225-54del (COL18A1) NP_085059.2:n.4225-164_4225-54del
NM_130444.3:c.4930-164_4930-54del (COL18A1) NP_569711.2:n.4930-164_4930-54del
NM_130445.4:c.3685-164_3685-54del (COL18A1) NP_569712.2:n.3685-164_3685-54del
NM_001379500.1:c.3694-164_3694-54del (COL18A1) MANE Select NP_001366429.1:n.3694-164_3694-54del