Canonical Allele Identifier: CA291547390

Gene: COL1A1

Linked Data

• ClinVar Variation Id: 425590
• ClinVar RCV Id: RCV000490718
• dbSNP Id: rs72645334
• MyVariant Identifiers: chr17:g.48273995C>T (hg19) ; chr17:g.50196634C>T (hg38)
• PubMed: PMID:25944380

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50196634C>T , CM000679.2:g.50196634C>T	GRCh38
NC_000017.10:g.48273995C>T , CM000679.1:g.48273995C>T	GRCh37
NC_000017.9:g.45628994C>T	NCBI36
NG_007400.1:g.10006G>A , LRG_1:g.10006G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.841G>A MANE Select	ENSP00000225964.6:p.Gly281Ser
ENST00000225964.9:c.841G>A	ENSP00000225964.5:p.Gly281Ser
ENST00000495677.1:n.568G>A
NM_000088.3:c.841G>A , LRG_1t1:c.841G>A	NP_000079.2:p.Gly281Ser
XM_005257058.3:c.841G>A	XP_005257115.2:p.Gly281Ser
XM_005257059.3:c.841G>A	XP_005257116.2:p.Gly281Ser
XM_011524341.1:c.841G>A	XP_011522643.1:p.Gly281Ser
XM_005257058.4:c.841G>A	XP_005257115.2:p.Gly281Ser
XM_005257059.4:c.841G>A	XP_005257116.2:p.Gly281Ser
NM_000088.4:c.841G>A MANE Select	NP_000079.2:p.Gly281Ser