Canonical Allele Identifier: CA2654916718
Gene: COL18A1 HGNC NCBI
SLC19A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45503838_45503841del , CM000683.2:g.45503838_45503841del GRCh38
NC_000021.8:g.46923752_46923755del , CM000683.1:g.46923752_46923755del GRCh37
NC_000021.7:g.45748180_45748183del NCBI36
NG_011903.1:g.103656_103659del
NG_028278.2:g.64305_64308del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355480.10:c.3224-173_3224-170del (COL18A1) ENSP00000347665.5:n.3224-173_3224-170del
ENST00000651438.1:c.2684-173_2684-170del (COL18A1) MANE Select ENSP00000498485.1:n.2684-173_2684-170del
ENST00000342220.9:c.725-173_725-170del (COL18A1) ENSP00000339118.5:n.725-173_725-170del
ENST00000355480.9:c.3224-173_3224-170del (COL18A1) ENSP00000347665.5:n.3224-173_3224-170del
ENST00000359759.8:c.3929-173_3929-170del (COL18A1) ENSP00000352798.4:n.3929-173_3929-170del
ENST00000400337.6:c.2684-173_2684-170del (COL18A1) ENSP00000383191.2:n.2684-173_2684-170del
ENST00000417954.5:c.498-5227_498-5224del (SLC19A1)
ENST00000461785.1:n.189+94_189+97del (SLC19A1)
ENST00000567670.5:c.1294-5227_1294-5224del (SLC19A1) ENSP00000457278.1:n.1294-5227_1294-5224del
NM_030582.3:c.3224-173_3224-170del (COL18A1) NP_085059.2:n.3224-173_3224-170del
NM_130444.2:c.3929-173_3929-170del (COL18A1) NP_569711.2:n.3929-173_3929-170del
NM_130445.3:c.2684-173_2684-170del (COL18A1) NP_569712.2:n.2684-173_2684-170del
XM_011529707.1:c.1585-870_1585-867del (SLC19A1) XP_011528009.1:n.1585-870_1585-867del
XM_017028445.2:c.1585-870_1585-867del (SLC19A1) XP_016883934.1:n.1585-870_1585-867del
NM_030582.4:c.3224-173_3224-170del (COL18A1) NP_085059.2:n.3224-173_3224-170del
NM_130444.3:c.3929-173_3929-170del (COL18A1) NP_569711.2:n.3929-173_3929-170del
NM_130445.4:c.2684-173_2684-170del (COL18A1) NP_569712.2:n.2684-173_2684-170del
NM_001379500.1:c.2684-173_2684-170del (COL18A1) MANE Select NP_001366429.1:n.2684-173_2684-170del