Canonical Allele Identifier: CA10065901

Gene: COL18A1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45475536G>T , CM000683.2:g.45475536G>T	GRCh38
NC_000021.8:g.46895450G>T , CM000683.1:g.46895450G>T	GRCh37
NC_000021.7:g.45719878G>T	NCBI36
NG_011903.1:g.75354G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001379500.1:c.798+1G>T MANE Select	NP_001366429.1:n.798+1G>T
ENST00000651438.1:c.798+1G>T MANE Select	ENSP00000498485.1:n.798+1G>T
NM_030582.3:c.1338+1G>T	NP_085059.2:n.1338+1G>T
NM_030582.4:c.1338+1G>T	NP_085059.2:n.1338+1G>T
NM_130444.2:c.2043+1G>T	NP_569711.2:n.2043+1G>T
NM_130444.3:c.2043+1G>T	NP_569711.2:n.2043+1G>T
NM_130445.3:c.798+1G>T	NP_569712.2:n.798+1G>T
NM_130445.4:c.798+1G>T	NP_569712.2:n.798+1G>T
ENST00000355480.10:c.1338+1G>T	ENSP00000347665.5:n.1338+1G>T
ENST00000355480.9:c.1338+1G>T	ENSP00000347665.5:n.1338+1G>T
ENST00000359759.8:c.2043+1G>T	ENSP00000352798.4:n.2043+1G>T
ENST00000400337.6:c.798+1G>T	ENSP00000383191.2:n.798+1G>T