Canonical Allele Identifier: CA14864951
Gene: COL18A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45468065A>T , CM000683.2:g.45468065A>T GRCh38
NC_000021.8:g.46887979A>T , CM000683.1:g.46887979A>T GRCh37
NC_000021.7:g.45712407A>T NCBI36
NG_011903.1:g.67883A>T

Transcript Alleles

HGVS Amino-acid Change
NM_001379500.1:c.107-177A>T MANE Select NP_001366429.1:n.107-177A>T
ENST00000651438.1:c.107-177A>T MANE Select ENSP00000498485.1:n.107-177A>T
NM_030582.3:c.647-177A>T NP_085059.2:n.647-177A>T
NM_030582.4:c.647-177A>T NP_085059.2:n.647-177A>T
NM_130444.2:c.1352-177A>T NP_569711.2:n.1352-177A>T
NM_130444.3:c.1352-177A>T NP_569711.2:n.1352-177A>T
NM_130445.3:c.107-177A>T NP_569712.2:n.107-177A>T
NM_130445.4:c.107-177A>T NP_569712.2:n.107-177A>T
ENST00000355480.10:c.647-177A>T ENSP00000347665.5:n.647-177A>T
ENST00000355480.9:c.647-177A>T ENSP00000347665.5:n.647-177A>T
ENST00000359759.8:c.1352-177A>T ENSP00000352798.4:n.1352-177A>T
ENST00000400337.6:c.107-177A>T ENSP00000383191.2:n.107-177A>T