Canonical Allele Identifier: CA2263917534
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50192690G= , CM000679.2:g.50192690G= GRCh38
NC_000017.10:g.48270051G= , CM000679.1:g.48270051G= GRCh37
NC_000017.9:g.45625050G= NCBI36
NG_007400.1:g.13950C= , LRG_1:g.13950C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1879C= MANE Select ENSP00000225964.6:p.Pro627=
ENST00000225964.9:c.1879C= ENSP00000225964.5:p.Pro627=
ENST00000476387.1:n.228C=
NM_000088.3:c.1879C= , LRG_1t1:c.1879C= NP_000079.2:p.Pro627=
XM_005257058.3:c.1879C= XP_005257115.2:p.Pro627=
XM_005257059.3:c.961C= XP_005257116.2:p.Pro321=
XM_011524341.1:c.1681C= XP_011522643.1:p.Pro561=
XM_005257058.4:c.1879C= XP_005257115.2:p.Pro627=
XM_005257059.4:c.961C= XP_005257116.2:p.Pro321=
NM_000088.4:c.1879C= MANE Select NP_000079.2:p.Pro627=