Canonical Allele Identifier: CA500848482

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48271355A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50193994A>T , CM000679.2:g.50193994A>T	GRCh38
NC_000017.10:g.48271355A>T , CM000679.1:g.48271355A>T	GRCh37
NC_000017.9:g.45626354A>T	NCBI36
NG_007400.1:g.12646T>A , LRG_1:g.12646T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.1716T>A MANE Select	ENSP00000225964.6:p.Gly572=
ENST00000225964.9:c.1716T>A	ENSP00000225964.5:p.Gly572=
ENST00000463440.1:n.106T>A
ENST00000471344.1:n.748T>A
ENST00000476387.1:n.65T>A
NM_000088.3:c.1716T>A , LRG_1t1:c.1716T>A	NP_000079.2:p.Gly572=
XM_005257058.3:c.1716T>A	XP_005257115.2:p.Gly572=
XM_005257059.3:c.958-1301T>A	XP_005257116.2:n.958-1301T>A
XM_011524341.1:c.1518T>A	XP_011522643.1:p.Gly506=
XM_005257058.4:c.1716T>A	XP_005257115.2:p.Gly572=
XM_005257059.4:c.958-1301T>A	XP_005257116.2:n.958-1301T>A
NM_000088.4:c.1716T>A MANE Select	NP_000079.2:p.Gly572=