Canonical Allele Identifier: CA291547228

Gene: COL1A1

Linked Data

• ClinVar Variation Id: 1432099
• ClinVar RCV Id: RCV001941098
• dbSNP Id: rs68062484
• MyVariant Identifiers: chr17:g.48273719C>T (hg19) ; chr17:g.50196358C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50196358C>T , CM000679.2:g.50196358C>T	GRCh38
NC_000017.10:g.48273719C>T , CM000679.1:g.48273719C>T	GRCh37
NC_000017.9:g.45628718C>T	NCBI36
NG_007400.1:g.10282G>A , LRG_1:g.10282G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.913G>A MANE Select	ENSP00000225964.6:p.Gly305Ser
ENST00000225964.9:c.913G>A	ENSP00000225964.5:p.Gly305Ser
ENST00000485870.1:n.238G>A
NM_000088.3:c.913G>A , LRG_1t1:c.913G>A	NP_000079.2:p.Gly305Ser
XM_005257058.3:c.913G>A	XP_005257115.2:p.Gly305Ser
XM_005257059.3:c.913G>A	XP_005257116.2:p.Gly305Ser
XM_011524341.1:c.913G>A	XP_011522643.1:p.Gly305Ser
XM_005257058.4:c.913G>A	XP_005257115.2:p.Gly305Ser
XM_005257059.4:c.913G>A	XP_005257116.2:p.Gly305Ser
NM_000088.4:c.913G>A MANE Select	NP_000079.2:p.Gly305Ser