Canonical Allele Identifier: CA2263917789
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50193635C= , CM000679.2:g.50193635C= GRCh38
NC_000017.10:g.48270996C= , CM000679.1:g.48270996C= GRCh37
NC_000017.9:g.45625995C= NCBI36
NG_007400.1:g.13005G= , LRG_1:g.13005G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1767+308G= MANE Select ENSP00000225964.6:n.1767+308G=
ENST00000225964.9:c.1767+308G= ENSP00000225964.5:n.1767+308G=
ENST00000463440.1:n.465G=
ENST00000471344.1:n.1107G=
ENST00000476387.1:n.116+308G=
NM_000088.3:c.1767+308G= , LRG_1t1:c.1767+308G= NP_000079.2:n.1767+308G=
XM_005257058.3:c.1767+308G= XP_005257115.2:n.1767+308G=
XM_005257059.3:c.958-942G= XP_005257116.2:n.958-942G=
XM_011524341.1:c.1569+308G= XP_011522643.1:n.1569+308G=
XM_005257058.4:c.1767+308G= XP_005257115.2:n.1767+308G=
XM_005257059.4:c.958-942G= XP_005257116.2:n.958-942G=
NM_000088.4:c.1767+308G= MANE Select NP_000079.2:n.1767+308G=