Canonical Allele Identifier: CA2263919176
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50196288_50196289delinsTC , CM000679.2:g.50196288_50196289delinsTC GRCh38
NC_000017.10:g.48273649_48273650delinsTC , CM000679.1:g.48273649_48273650delinsTC GRCh37
NC_000017.9:g.45628648_45628649delinsTC NCBI36
NG_007400.1:g.10351_10352delinsGA , LRG_1:g.10351_10352delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.957+25_957+26delinsGA MANE Select ENSP00000225964.6:n.957+25_957+26delinsGA
ENST00000225964.9:c.957+25_957+26delinsGA ENSP00000225964.5:n.957+25_957+26delinsGA
ENST00000485870.1:n.282+25_282+26delinsGA
NM_000088.3:c.957+25_957+26delinsGA , LRG_1t1:c.957+25_957+26delinsGA NP_000079.2:n.957+25_957+26delinsGA
XM_005257058.3:c.957+25_957+26delinsGA XP_005257115.2:n.957+25_957+26delinsGA
XM_005257059.3:c.957+25_957+26delinsGA XP_005257116.2:n.957+25_957+26delinsGA
XM_011524341.1:c.957+25_957+26delinsGA XP_011522643.1:n.957+25_957+26delinsGA
XM_005257058.4:c.957+25_957+26delinsGA XP_005257115.2:n.957+25_957+26delinsGA
XM_005257059.4:c.957+25_957+26delinsGA XP_005257116.2:n.957+25_957+26delinsGA
NM_000088.4:c.957+25_957+26delinsGA MANE Select NP_000079.2:n.957+25_957+26delinsGA