Canonical Allele Identifier: CA1726750773
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94409373_94409376delinsCGTG , CM000669.2:g.94409373_94409376delinsCGTG GRCh38
NC_000007.13:g.94038685_94038688delinsCGTG , CM000669.1:g.94038685_94038688delinsCGTG GRCh37
NC_000007.12:g.93876621_93876624delinsCGTG NCBI36
NG_007405.1:g.19813_19816delinsCGTG , LRG_2:g.19813_19816delinsCGTG

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.844_847delinsCGTG MANE Select ENSP00000297268.6:p.Arg282=
ENST00000297268.10:c.844_847delinsCGTG ENSP00000297268.6:p.Arg282=
ENST00000620463.1:c.838_841delinsCGTG ENSP00000477719.1:p.Arg280=
NM_000089.3:c.844_847delinsCGTG , LRG_2t1:c.844_847delinsCGTG NP_000080.2:p.Arg282=
NM_000089.4:c.844_847delinsCGTG MANE Select NP_000080.2:p.Arg282=