Canonical Allele Identifier: CA400215625

Gene: COL1A1

Linked Data

• ClinVar Variation Id: 2572828
• ClinVar RCV Id: RCV003314942
• MyVariant Identifiers: chr17:g.48271401C>T (hg19) ; chr17:g.50194040C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50194040C>T , CM000679.2:g.50194040C>T	GRCh38
NC_000017.10:g.48271401C>T , CM000679.1:g.48271401C>T	GRCh37
NC_000017.9:g.45626400C>T	NCBI36
NG_007400.1:g.12600G>A , LRG_1:g.12600G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.1670G>A MANE Select	ENSP00000225964.6:p.Gly557Asp
ENST00000225964.9:c.1670G>A	ENSP00000225964.5:p.Gly557Asp
ENST00000463440.1:n.60G>A
ENST00000471344.1:n.702G>A
ENST00000476387.1:n.19G>A
NM_000088.3:c.1670G>A , LRG_1t1:c.1670G>A	NP_000079.2:p.Gly557Asp
XM_005257058.3:c.1670G>A	XP_005257115.2:p.Gly557Asp
XM_005257059.3:c.958-1347G>A	XP_005257116.2:n.958-1347G>A
XM_011524341.1:c.1472G>A	XP_011522643.1:p.Gly491Asp
XM_005257058.4:c.1670G>A	XP_005257115.2:p.Gly557Asp
XM_005257059.4:c.958-1347G>A	XP_005257116.2:n.958-1347G>A
NM_000088.4:c.1670G>A MANE Select	NP_000079.2:p.Gly557Asp