Canonical Allele Identifier: CA400215433

Gene: COL1A1

Linked Data

• COSMIC: COSM3519044
• MyVariant Identifiers: chr17:g.48271366C>T (hg19) ; chr17:g.50194005C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.1705G>A MANE Select	ENSP00000225964.6:p.Gly569Ser
ENST00000225964.9:c.1705G>A	ENSP00000225964.5:p.Gly569Ser
ENST00000463440.1:n.95G>A
ENST00000471344.1:n.737G>A
ENST00000476387.1:n.54G>A
NM_000088.3:c.1705G>A , LRG_1t1:c.1705G>A	NP_000079.2:p.Gly569Ser
XM_005257058.3:c.1705G>A	XP_005257115.2:p.Gly569Ser
XM_005257059.3:c.958-1312G>A	XP_005257116.2:n.958-1312G>A
XM_011524341.1:c.1507G>A	XP_011522643.1:p.Gly503Ser
XM_005257058.4:c.1705G>A	XP_005257115.2:p.Gly569Ser
XM_005257059.4:c.958-1312G>A	XP_005257116.2:n.958-1312G>A
NM_000088.4:c.1705G>A MANE Select	NP_000079.2:p.Gly569Ser