Canonical Allele Identifier: CA1022830487
Gene: COL18A1 HGNC NCBI
SLC19A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45510949_45511071del , CM000683.2:g.45510949_45511071del GRCh38
NC_000021.8:g.46930863_46930985del , CM000683.1:g.46930863_46930985del GRCh37
NC_000021.7:g.45755291_45755413del NCBI36
NG_011903.1:g.110758_110880del
NG_028278.2:g.57080_57202del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355480.10:c.4234-162_4234-40del (COL18A1) ENSP00000347665.5:n.4234-162_4234-40del
ENST00000651438.1:c.3694-162_3694-40del (COL18A1) MANE Select ENSP00000498485.1:n.3694-162_3694-40del
ENST00000342220.9:c.1738-162_1738-40del (COL18A1) ENSP00000339118.5:n.1738-162_1738-40del
ENST00000355480.9:c.4234-162_4234-40del (COL18A1) ENSP00000347665.5:n.4234-162_4234-40del
ENST00000359759.8:c.4939-162_4939-40del (COL18A1) ENSP00000352798.4:n.4939-162_4939-40del
ENST00000400337.6:c.3694-162_3694-40del (COL18A1) ENSP00000383191.2:n.3694-162_3694-40del
ENST00000417954.5:c.498-12452_498-12330del (SLC19A1)
ENST00000423214.1:c.648-162_648-40del (COL18A1)
ENST00000473212.1:n.2020-162_2020-40del (COL18A1)
ENST00000567670.5:c.1294-12452_1294-12330del (SLC19A1) ENSP00000457278.1:n.1294-12452_1294-12330del
NM_030582.3:c.4225-162_4225-40del (COL18A1) NP_085059.2:n.4225-162_4225-40del
NM_130444.2:c.4930-162_4930-40del (COL18A1) NP_569711.2:n.4930-162_4930-40del
NM_130445.3:c.3685-162_3685-40del (COL18A1) NP_569712.2:n.3685-162_3685-40del
XM_011529707.1:c.1585-8095_1585-7973del (SLC19A1) XP_011528009.1:n.1585-8095_1585-7973del
XM_017028445.2:c.1585-8095_1585-7973del (SLC19A1) XP_016883934.1:n.1585-8095_1585-7973del
NM_030582.4:c.4225-162_4225-40del (COL18A1) NP_085059.2:n.4225-162_4225-40del
NM_130444.3:c.4930-162_4930-40del (COL18A1) NP_569711.2:n.4930-162_4930-40del
NM_130445.4:c.3685-162_3685-40del (COL18A1) NP_569712.2:n.3685-162_3685-40del
NM_001379500.1:c.3694-162_3694-40del (COL18A1) MANE Select NP_001366429.1:n.3694-162_3694-40del