Canonical Allele Identifier: CA500841688
Gene: COL1A1 HGNC NCBI

Linked Data

dbSNP Id: rs1372138293

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50184491_50184492insG , CM000679.2:g.50184491_50184492insG GRCh38
NC_000017.10:g.48261852_48261853insG , CM000679.1:g.48261852_48261853insG GRCh37
NC_000017.9:g.45616851_45616852insG NCBI36
NG_007400.1:g.22148_22149insC , LRG_1:g.22148_22149insC

Transcript Alleles

HGVS Amino-acid change
ENST00000225964.10:c.*1010_*1011insC MANE Select ENSP00000225964.6:n.*1010_*1011insC
ENST00000225964.9:c.*1010_*1011insC ENSP00000225964.5:n.*1010_*1011insC
NM_000088.3:c.*1010_*1011insC , LRG_1t1:c.*1010_*1011insC NP_000079.2:n.*1010_*1011insC
XM_005257058.3:c.*1010_*1011insC XP_005257115.2:n.*1010_*1011insC
XM_005257059.3:c.*1010_*1011insC XP_005257116.2:n.*1010_*1011insC
XM_011524341.1:c.*1010_*1011insC XP_011522643.1:n.*1010_*1011insC
XM_005257058.4:c.*1010_*1011insC XP_005257115.2:n.*1010_*1011insC
XM_005257059.4:c.*1010_*1011insC XP_005257116.2:n.*1010_*1011insC
NM_000088.4:c.*1010_*1011insC MANE Select NP_000079.2:n.*1010_*1011insC