Canonical Allele Identifier: CA2263917795
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50193657A= , CM000679.2:g.50193657A= GRCh38
NC_000017.10:g.48271018A= , CM000679.1:g.48271018A= GRCh37
NC_000017.9:g.45626017A= NCBI36
NG_007400.1:g.12983T= , LRG_1:g.12983T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1767+286T= MANE Select ENSP00000225964.6:n.1767+286T=
ENST00000225964.9:c.1767+286T= ENSP00000225964.5:n.1767+286T=
ENST00000463440.1:n.443T=
ENST00000471344.1:n.1085T=
ENST00000476387.1:n.116+286T=
NM_000088.3:c.1767+286T= , LRG_1t1:c.1767+286T= NP_000079.2:n.1767+286T=
XM_005257058.3:c.1767+286T= XP_005257115.2:n.1767+286T=
XM_005257059.3:c.958-964T= XP_005257116.2:n.958-964T=
XM_011524341.1:c.1569+286T= XP_011522643.1:n.1569+286T=
XM_005257058.4:c.1767+286T= XP_005257115.2:n.1767+286T=
XM_005257059.4:c.958-964T= XP_005257116.2:n.958-964T=
NM_000088.4:c.1767+286T= MANE Select NP_000079.2:n.1767+286T=