Canonical Allele Identifier: CA500848289

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48270370T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50193009T>A , CM000679.2:g.50193009T>A	GRCh38
NC_000017.10:g.48270370T>A , CM000679.1:g.48270370T>A	GRCh37
NC_000017.9:g.45625369T>A	NCBI36
NG_007400.1:g.13631A>T , LRG_1:g.13631A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.1806A>T MANE Select	ENSP00000225964.6:p.Gly602=
ENST00000225964.9:c.1806A>T	ENSP00000225964.5:p.Gly602=
ENST00000476387.1:n.155A>T
NM_000088.3:c.1806A>T , LRG_1t1:c.1806A>T	NP_000079.2:p.Gly602=
XM_005257058.3:c.1806A>T	XP_005257115.2:p.Gly602=
XM_005257059.3:c.958-316A>T	XP_005257116.2:n.958-316A>T
XM_011524341.1:c.1608A>T	XP_011522643.1:p.Gly536=
XM_005257058.4:c.1806A>T	XP_005257115.2:p.Gly602=
XM_005257059.4:c.958-316A>T	XP_005257116.2:n.958-316A>T
NM_000088.4:c.1806A>T MANE Select	NP_000079.2:p.Gly602=