Canonical Allele Identifier: CA2392171578

Gene: COL18A1

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.45476383_45476384delinsAC , CM000683.2:g.45476383_45476384delinsAC	GRCh38
NC_000021.8:g.46896297_46896298delinsAC , CM000683.1:g.46896297_46896298delinsAC	GRCh37
NC_000021.7:g.45720725_45720726delinsAC	NCBI36
NG_011903.1:g.76201_76202delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000355480.10:c.1371_1372delinsAC	ENSP00000347665.5:p.Pro457=
ENST00000651438.1:c.831_832delinsAC MANE Select	ENSP00000498485.1:p.Pro277=
ENST00000355480.9:c.1371_1372delinsAC	ENSP00000347665.5:p.Pro457=
ENST00000359759.8:c.2076_2077delinsAC	ENSP00000352798.4:p.Pro692=
ENST00000400337.6:c.831_832delinsAC	ENSP00000383191.2:p.Pro277=
NM_030582.3:c.1371_1372delinsAC	NP_085059.2:p.Pro457=
NM_130444.2:c.2076_2077delinsAC	NP_569711.2:p.Pro692=
NM_130445.3:c.831_832delinsAC	NP_569712.2:p.Pro277=
NM_030582.4:c.1371_1372delinsAC	NP_085059.2:p.Pro457=
NM_130444.3:c.2076_2077delinsAC	NP_569711.2:p.Pro692=
NM_130445.4:c.831_832delinsAC	NP_569712.2:p.Pro277=
NM_001379500.1:c.831_832delinsAC MANE Select	NP_001366429.1:p.Pro277=