Canonical Allele Identifier: CA2263917961
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194005C= , CM000679.2:g.50194005C= GRCh38
NC_000017.10:g.48271366C= , CM000679.1:g.48271366C= GRCh37
NC_000017.9:g.45626365C= NCBI36
NG_007400.1:g.12635G= , LRG_1:g.12635G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1705G= MANE Select ENSP00000225964.6:p.Gly569=
ENST00000225964.9:c.1705G= ENSP00000225964.5:p.Gly569=
ENST00000463440.1:n.95G=
ENST00000471344.1:n.737G=
ENST00000476387.1:n.54G=
NM_000088.3:c.1705G= , LRG_1t1:c.1705G= NP_000079.2:p.Gly569=
XM_005257058.3:c.1705G= XP_005257115.2:p.Gly569=
XM_005257059.3:c.958-1312G= XP_005257116.2:n.958-1312G=
XM_011524341.1:c.1507G= XP_011522643.1:p.Gly503=
XM_005257058.4:c.1705G= XP_005257115.2:p.Gly569=
XM_005257059.4:c.958-1312G= XP_005257116.2:n.958-1312G=
NM_000088.4:c.1705G= MANE Select NP_000079.2:p.Gly569=