Canonical Allele Identifier: CA1726776158
Gene: COL1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1792194383

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94422813_94422814del , CM000669.2:g.94422813_94422814del GRCh38
NC_000007.13:g.94052125_94052126del , CM000669.1:g.94052125_94052126del GRCh37
NC_000007.12:g.93890061_93890062del NCBI36
NG_007405.1:g.33253_33254del , LRG_2:g.33253_33254del

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.2404-144_2404-143del MANE Select ENSP00000297268.6:n.2404-144_2404-143del
ENST00000297268.10:c.2404-144_2404-143del ENSP00000297268.6:n.2404-144_2404-143del
ENST00000481570.5:n.343_344del
ENST00000497316.5:n.801-144_801-143del
ENST00000620463.1:c.2398-144_2398-143del ENSP00000477719.1:n.2398-144_2398-143del
NM_000089.3:c.2404-144_2404-143del , LRG_2t1:c.2404-144_2404-143del NP_000080.2:n.2404-144_2404-143del
NM_000089.4:c.2404-144_2404-143del MANE Select NP_000080.2:n.2404-144_2404-143del