Canonical Allele Identifier: CA2263917173
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50192959T= , CM000679.2:g.50192959T= GRCh38
NC_000017.10:g.48270320T= , CM000679.1:g.48270320T= GRCh37
NC_000017.9:g.45625319T= NCBI36
NG_007400.1:g.13681A= , LRG_1:g.13681A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1821+35A= MANE Select ENSP00000225964.6:n.1821+35A=
ENST00000225964.9:c.1821+35A= ENSP00000225964.5:n.1821+35A=
ENST00000476387.1:n.170+35A=
NM_000088.3:c.1821+35A= , LRG_1t1:c.1821+35A= NP_000079.2:n.1821+35A=
XM_005257058.3:c.1821+35A= XP_005257115.2:n.1821+35A=
XM_005257059.3:c.958-266A= XP_005257116.2:n.958-266A=
XM_011524341.1:c.1623+35A= XP_011522643.1:n.1623+35A=
XM_005257058.4:c.1821+35A= XP_005257115.2:n.1821+35A=
XM_005257059.4:c.958-266A= XP_005257116.2:n.958-266A=
NM_000088.4:c.1821+35A= MANE Select NP_000079.2:n.1821+35A=