Canonical Allele Identifier: CA2263920698
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50199405G= , CM000679.2:g.50199405G= GRCh38
NC_000017.10:g.48276766G= , CM000679.1:g.48276766G= GRCh37
NC_000017.9:g.45631765G= NCBI36
NG_007400.1:g.7235C= , LRG_1:g.7235C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.369+13C= MANE Select ENSP00000225964.6:n.369+13C=
ENST00000225964.9:c.369+13C= ENSP00000225964.5:n.369+13C=
ENST00000474644.1:n.590+13C=
ENST00000507689.1:c.423+13C= ENSP00000460459.1:n.423+13C=
NM_000088.3:c.369+13C= , LRG_1t1:c.369+13C= NP_000079.2:n.369+13C=
XM_005257058.3:c.369+13C= XP_005257115.2:n.369+13C=
XM_005257059.3:c.369+13C= XP_005257116.2:n.369+13C=
XM_011524341.1:c.369+13C= XP_011522643.1:n.369+13C=
XM_005257058.4:c.369+13C= XP_005257115.2:n.369+13C=
XM_005257059.4:c.369+13C= XP_005257116.2:n.369+13C=
NM_000088.4:c.369+13C= MANE Select NP_000079.2:n.369+13C=