Canonical Allele Identifier: CA2580077971
Gene: COL1A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1806455
ClinVar RCV Id: RCV002472338

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94409371_94409388dup , CM000669.2:g.94409371_94409388dup GRCh38
NC_000007.13:g.94038683_94038700dup , CM000669.1:g.94038683_94038700dup GRCh37
NC_000007.12:g.93876619_93876636dup NCBI36
NG_007405.1:g.19811_19828dup , LRG_2:g.19811_19828dup

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.842_859dup MANE Select ENSP00000297268.6:p.Gly286_Leu287insProAr...
ENST00000297268.10:c.842_859dup ENSP00000297268.6:p.Gly286_Leu287insProAr...
ENST00000620463.1:c.836_853dup ENSP00000477719.1:p.Gly284_Leu285insProAr...
NM_000089.3:c.842_859dup , LRG_2t1:c.842_859dup NP_000080.2:p.Gly286_Leu287insProArgGlyGl...
NM_000089.4:c.842_859dup MANE Select NP_000080.2:p.Gly286_Leu287insProArgGlyGl...