Canonical Allele Identifier: CA2580078009
Gene: COL1A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2156186
ClinVar RCV Id: RCV003075331

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94413926_94413927delinsTG , CM000669.2:g.94413926_94413927delinsTG GRCh38
NC_000007.13:g.94043238_94043239delinsTG , CM000669.1:g.94043238_94043239delinsTG GRCh37
NC_000007.12:g.93881174_93881175delinsTG NCBI36
NG_007405.1:g.24366_24367delinsTG , LRG_2:g.24366_24367delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.1644_1645delinsTG MANE Select ENSP00000297268.6:p.Pro549Ala
ENST00000297268.10:c.1644_1645delinsTG ENSP00000297268.6:p.Pro549Ala
ENST00000488298.5:n.68_69delinsTG
ENST00000620463.1:c.1638_1639delinsTG ENSP00000477719.1:p.Pro547Ala
NM_000089.3:c.1644_1645delinsTG , LRG_2t1:c.1644_1645delinsTG NP_000080.2:p.Pro549Ala
NM_000089.4:c.1644_1645delinsTG MANE Select NP_000080.2:p.Pro549Ala