Canonical Allele Identifier: CA291545076

Gene: COL1A1

Linked Data

• dbSNP Id: rs72648362
• MyVariant Identifiers: chr17:g.48271404T>C (hg19) ; chr17:g.50194043T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50194043T>C , CM000679.2:g.50194043T>C	GRCh38
NC_000017.10:g.48271404T>C , CM000679.1:g.48271404T>C	GRCh37
NC_000017.9:g.45626403T>C	NCBI36
NG_007400.1:g.12597A>G , LRG_1:g.12597A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.1669-2A>G MANE Select	ENSP00000225964.6:n.1669-2A>G
ENST00000225964.9:c.1669-2A>G	ENSP00000225964.5:n.1669-2A>G
ENST00000463440.1:n.59-2A>G
ENST00000471344.1:n.699A>G
ENST00000476387.1:n.16A>G
NM_000088.3:c.1669-2A>G , LRG_1t1:c.1669-2A>G	NP_000079.2:n.1669-2A>G
XM_005257058.3:c.1669-2A>G	XP_005257115.2:n.1669-2A>G
XM_005257059.3:c.958-1350A>G	XP_005257116.2:n.958-1350A>G
XM_011524341.1:c.1471-2A>G	XP_011522643.1:n.1471-2A>G
XM_005257058.4:c.1669-2A>G	XP_005257115.2:n.1669-2A>G
XM_005257059.4:c.958-1350A>G	XP_005257116.2:n.958-1350A>G
NM_000088.4:c.1669-2A>G MANE Select	NP_000079.2:n.1669-2A>G