Canonical Allele Identifier: CA2654909327
Gene: COL18A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45476269_45476284del , CM000683.2:g.45476269_45476284del GRCh38
NC_000021.8:g.46896183_46896198del , CM000683.1:g.46896183_46896198del GRCh37
NC_000021.7:g.45720611_45720626del NCBI36
NG_011903.1:g.76087_76102del

Transcript Alleles

HGVS Amino-acid change
ENST00000355480.10:c.1339-82_1339-67del ENSP00000347665.5:n.1339-82_1339-67del
ENST00000651438.1:c.799-82_799-67del MANE Select ENSP00000498485.1:n.799-82_799-67del
ENST00000355480.9:c.1339-82_1339-67del ENSP00000347665.5:n.1339-82_1339-67del
ENST00000359759.8:c.2044-82_2044-67del ENSP00000352798.4:n.2044-82_2044-67del
ENST00000400337.6:c.799-82_799-67del ENSP00000383191.2:n.799-82_799-67del
NM_030582.3:c.1339-82_1339-67del NP_085059.2:n.1339-82_1339-67del
NM_130444.2:c.2044-82_2044-67del NP_569711.2:n.2044-82_2044-67del
NM_130445.3:c.799-82_799-67del NP_569712.2:n.799-82_799-67del
NM_030582.4:c.1339-82_1339-67del NP_085059.2:n.1339-82_1339-67del
NM_130444.3:c.2044-82_2044-67del NP_569711.2:n.2044-82_2044-67del
NM_130445.4:c.799-82_799-67del NP_569712.2:n.799-82_799-67del
NM_001379500.1:c.799-82_799-67del MANE Select NP_001366429.1:n.799-82_799-67del