Canonical Allele Identifier: CA291544424

Gene: COL1A1

Linked Data

• dbSNP Id: rs143145612
• COSMIC: COSM107091
• MyVariant Identifiers: chr17:g.48270196C>T (hg19) ; chr17:g.50192835C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50192835C>T , CM000679.2:g.50192835C>T	GRCh38
NC_000017.10:g.48270196C>T , CM000679.1:g.48270196C>T	GRCh37
NC_000017.9:g.45625195C>T	NCBI36
NG_007400.1:g.13805G>A , LRG_1:g.13805G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.1837G>A MANE Select	ENSP00000225964.6:p.Asp613Asn
ENST00000225964.9:c.1837G>A	ENSP00000225964.5:p.Asp613Asn
ENST00000476387.1:n.186G>A
NM_000088.3:c.1837G>A , LRG_1t1:c.1837G>A	NP_000079.2:p.Asp613Asn
XM_005257058.3:c.1837G>A	XP_005257115.2:p.Asp613Asn
XM_005257059.3:c.958-142G>A	XP_005257116.2:n.958-142G>A
XM_011524341.1:c.1639G>A	XP_011522643.1:p.Asp547Asn
XM_005257058.4:c.1837G>A	XP_005257115.2:p.Asp613Asn
XM_005257059.4:c.958-142G>A	XP_005257116.2:n.958-142G>A
NM_000088.4:c.1837G>A MANE Select	NP_000079.2:p.Asp613Asn