Canonical Allele Identifier: CA918076055
Gene: COL1A2 HGNC NCBI

Linked Data

dbSNP Id: rs869112106

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94423073_94423074dup , CM000669.2:g.94423073_94423074dup GRCh38
NC_000007.13:g.94052385_94052386dup , CM000669.1:g.94052385_94052386dup GRCh37
NC_000007.12:g.93890321_93890322dup NCBI36
NG_007405.1:g.33513_33514dup , LRG_2:g.33513_33514dup

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.2520_2521dup MANE Select ENSP00000297268.6:p.Gly841ValfsTer?
ENST00000297268.10:c.2520_2521dup ENSP00000297268.6:p.Gly841ValfsTer?
ENST00000481570.5:n.603_604dup
ENST00000497316.5:n.917_918dup
ENST00000620463.1:c.2514_2515dup ENSP00000477719.1:p.Gly839ValfsTer?
NM_000089.3:c.2520_2521dup , LRG_2t1:c.2520_2521dup NP_000080.2:p.Gly841ValfsTer?
NM_000089.4:c.2520_2521dup MANE Select NP_000080.2:p.Gly841ValfsTer?