Canonical Allele Identifier: CA2695226629
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50192694_50192695delinsAG , CM000679.2:g.50192694_50192695delinsAG GRCh38
NC_000017.10:g.48270055_48270056delinsAG , CM000679.1:g.48270055_48270056delinsAG GRCh37
NC_000017.9:g.45625054_45625055delinsAG NCBI36
NG_007400.1:g.13945_13946delinsCT , LRG_1:g.13945_13946delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1876-2_1876-1delinsCT MANE Select ENSP00000225964.6:n.1876-2_1876-1delinsCT
ENST00000225964.9:c.1876-2_1876-1delinsCT ENSP00000225964.5:n.1876-2_1876-1delinsCT
ENST00000476387.1:n.225-2_225-1delinsCT
NM_000088.3:c.1876-2_1876-1delinsCT , LRG_1t1:c.1876-2_1876-1delinsCT NP_000079.2:n.1876-2_1876-1delinsCT
XM_005257058.3:c.1876-2_1876-1delinsCT XP_005257115.2:n.1876-2_1876-1delinsCT
XM_005257059.3:c.958-2_958-1delinsCT XP_005257116.2:n.958-2_958-1delinsCT
XM_011524341.1:c.1678-2_1678-1delinsCT XP_011522643.1:n.1678-2_1678-1delinsCT
XM_005257058.4:c.1876-2_1876-1delinsCT XP_005257115.2:n.1876-2_1876-1delinsCT
XM_005257059.4:c.958-2_958-1delinsCT XP_005257116.2:n.958-2_958-1delinsCT
NM_000088.4:c.1876-2_1876-1delinsCT MANE Select NP_000079.2:n.1876-2_1876-1delinsCT