Canonical Allele Identifier: CA400223887

Gene: COL1A1

Linked Data

• ClinVar Variation Id: 1451481
• ClinVar RCV Id: RCV002007244
• dbSNP Id: rs72645321
• MyVariant Identifiers: chr17:g.48274406C>G (hg19) ; chr17:g.50197045C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50197045C>G , CM000679.2:g.50197045C>G	GRCh38
NC_000017.10:g.48274406C>G , CM000679.1:g.48274406C>G	GRCh37
NC_000017.9:g.45629405C>G	NCBI36
NG_007400.1:g.9595G>C , LRG_1:g.9595G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.769G>C MANE Select	ENSP00000225964.6:p.Gly257Arg
ENST00000225964.9:c.769G>C	ENSP00000225964.5:p.Gly257Arg
ENST00000495677.1:n.496G>C
NM_000088.3:c.769G>C , LRG_1t1:c.769G>C	NP_000079.2:p.Gly257Arg
XM_005257058.3:c.769G>C	XP_005257115.2:p.Gly257Arg
XM_005257059.3:c.769G>C	XP_005257116.2:p.Gly257Arg
XM_011524341.1:c.769G>C	XP_011522643.1:p.Gly257Arg
XM_005257058.4:c.769G>C	XP_005257115.2:p.Gly257Arg
XM_005257059.4:c.769G>C	XP_005257116.2:p.Gly257Arg
NM_000088.4:c.769G>C MANE Select	NP_000079.2:p.Gly257Arg