Canonical Allele Identifier: CA2392171581

Gene: COL18A1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45476387C= , CM000683.2:g.45476387C=	GRCh38
NC_000021.8:g.46896301C= , CM000683.1:g.46896301C=	GRCh37
NC_000021.7:g.45720729C=	NCBI36
NG_011903.1:g.76205C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355480.10:c.1375C=	ENSP00000347665.5:p.Pro459=
ENST00000651438.1:c.835C= MANE Select	ENSP00000498485.1:p.Pro279=
ENST00000355480.9:c.1375C=	ENSP00000347665.5:p.Pro459=
ENST00000359759.8:c.2080C=	ENSP00000352798.4:p.Pro694=
ENST00000400337.6:c.835C=	ENSP00000383191.2:p.Pro279=
NM_030582.3:c.1375C=	NP_085059.2:p.Pro459=
NM_130444.2:c.2080C=	NP_569711.2:p.Pro694=
NM_130445.3:c.835C=	NP_569712.2:p.Pro279=
NM_030582.4:c.1375C=	NP_085059.2:p.Pro459=
NM_130444.3:c.2080C=	NP_569711.2:p.Pro694=
NM_130445.4:c.835C=	NP_569712.2:p.Pro279=
NM_001379500.1:c.835C= MANE Select	NP_001366429.1:p.Pro279=