Canonical Allele Identifier: CA2392191283
Gene: COL18A1 HGNC NCBI
SLC19A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45505243_45505244delinsCA , CM000683.2:g.45505243_45505244delinsCA GRCh38
NC_000021.8:g.46925157_46925158delinsCA , CM000683.1:g.46925157_46925158delinsCA GRCh37
NC_000021.7:g.45749585_45749586delinsCA NCBI36
NG_011903.1:g.105052_105053delinsCA
NG_028278.2:g.62900_62901delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000355480.10:c.3518_3519delinsCA (COL18A1) ENSP00000347665.5:p.Pro1173=
ENST00000651438.1:c.2978_2979delinsCA (COL18A1) MANE Select ENSP00000498485.1:p.Pro993=
ENST00000342220.9:c.1019_1020delinsCA (COL18A1) ENSP00000339118.5:p.Pro340=
ENST00000355480.9:c.3518_3519delinsCA (COL18A1) ENSP00000347665.5:p.Pro1173=
ENST00000359759.8:c.4223_4224delinsCA (COL18A1) ENSP00000352798.4:p.Pro1408=
ENST00000400337.6:c.2978_2979delinsCA (COL18A1) ENSP00000383191.2:p.Pro993=
ENST00000417954.5:c.498-6632_498-6631delinsTG (SLC19A1)
ENST00000567670.5:c.1294-6632_1294-6631delinsTG (SLC19A1) ENSP00000457278.1:n.1294-6632_1294-6631de...
NM_030582.3:c.3509_3510delinsCA (COL18A1) NP_085059.2:p.Pro1170=
NM_130444.2:c.4214_4215delinsCA (COL18A1) NP_569711.2:p.Pro1405=
NM_130445.3:c.2969_2970delinsCA (COL18A1) NP_569712.2:p.Pro990=
XM_011529707.1:c.1585-2275_1585-2274delinsTG (SLC19A1) XP_011528009.1:n.1585-2275_1585-2274delin...
XM_017028445.2:c.1585-2275_1585-2274delinsTG (SLC19A1) XP_016883934.1:n.1585-2275_1585-2274delin...
NM_030582.4:c.3509_3510delinsCA (COL18A1) NP_085059.2:p.Pro1170=
NM_130444.3:c.4214_4215delinsCA (COL18A1) NP_569711.2:p.Pro1405=
NM_130445.4:c.2969_2970delinsCA (COL18A1) NP_569712.2:p.Pro990=
NM_001379500.1:c.2978_2979delinsCA (COL18A1) MANE Select NP_001366429.1:p.Pro993=