Canonical Allele Identifier: CA10066105
Gene: COL18A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.45477960G>A , CM000683.2:g.45477960G>A GRCh38
NC_000021.8:g.46897874G>A , CM000683.1:g.46897874G>A GRCh37
NC_000021.7:g.45722302G>A NCBI36
NG_011903.1:g.77778G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355480.10:c.1756G>A ENSP00000347665.5:p.Glu586Lys
ENST00000651438.1:c.1216G>A MANE Select ENSP00000498485.1:p.Glu406Lys
ENST00000355480.9:c.1756G>A ENSP00000347665.5:p.Glu586Lys
ENST00000359759.8:c.2461G>A ENSP00000352798.4:p.Glu821Lys
ENST00000400337.6:c.1216G>A ENSP00000383191.2:p.Glu406Lys
NM_030582.3:c.1756G>A NP_085059.2:p.Glu586Lys
NM_130444.2:c.2461G>A NP_569711.2:p.Glu821Lys
NM_130445.3:c.1216G>A NP_569712.2:p.Glu406Lys
NM_030582.4:c.1756G>A NP_085059.2:p.Glu586Lys
NM_130444.3:c.2461G>A NP_569711.2:p.Glu821Lys
NM_130445.4:c.1216G>A NP_569712.2:p.Glu406Lys
NM_001379500.1:c.1216G>A MANE Select NP_001366429.1:p.Glu406Lys