Canonical Allele Identifier: CA2739268226

Gene: COL1A1

Linked Data

• ClinVar Variation Id: 2818008
• ClinVar RCV Id: RCV003631729

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50194121G>T , CM000679.2:g.50194121G>T	GRCh38
NC_000017.10:g.48271482G>T , CM000679.1:g.48271482G>T	GRCh37
NC_000017.9:g.45626481G>T	NCBI36
NG_007400.1:g.12519C>A , LRG_1:g.12519C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.1668+9C>A MANE Select	ENSP00000225964.6:n.1668+9C>A
ENST00000225964.9:c.1668+9C>A	ENSP00000225964.5:n.1668+9C>A
ENST00000463440.1:n.58+9C>A
ENST00000471344.1:n.621C>A
NM_000088.3:c.1668+9C>A , LRG_1t1:c.1668+9C>A	NP_000079.2:n.1668+9C>A
XM_005257058.3:c.1668+9C>A	XP_005257115.2:n.1668+9C>A
XM_005257059.3:c.958-1428C>A	XP_005257116.2:n.958-1428C>A
XM_011524341.1:c.1470+9C>A	XP_011522643.1:n.1470+9C>A
XM_005257058.4:c.1668+9C>A	XP_005257115.2:n.1668+9C>A
XM_005257059.4:c.958-1428C>A	XP_005257116.2:n.958-1428C>A
NM_000088.4:c.1668+9C>A MANE Select	NP_000079.2:n.1668+9C>A