Canonical Allele Identifier: CA8645225

Gene: COL1A1

Linked Data

• dbSNP Id: rs756823986
• ExAC: 17:48271915 G / C
• MyVariant Identifiers: chr17:g.48271915G>C (hg19) ; chr17:g.50194554G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50194554G>C , CM000679.2:g.50194554G>C	GRCh38
NC_000017.10:g.48271915G>C , CM000679.1:g.48271915G>C	GRCh37
NC_000017.9:g.45626914G>C	NCBI36
NG_007400.1:g.12086C>G , LRG_1:g.12086C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.1515+19C>G MANE Select	ENSP00000225964.6:n.1515+19C>G
ENST00000225964.9:c.1515+19C>G	ENSP00000225964.5:n.1515+19C>G
ENST00000471344.1:n.459+19C>G
NM_000088.3:c.1515+19C>G , LRG_1t1:c.1515+19C>G	NP_000079.2:n.1515+19C>G
XM_005257058.3:c.1515+19C>G	XP_005257115.2:n.1515+19C>G
XM_005257059.3:c.957+1760C>G	XP_005257116.2:n.957+1760C>G
XM_011524341.1:c.1317+19C>G	XP_011522643.1:n.1317+19C>G
XM_005257058.4:c.1515+19C>G	XP_005257115.2:n.1515+19C>G
XM_005257059.4:c.957+1760C>G	XP_005257116.2:n.957+1760C>G
NM_000088.4:c.1515+19C>G MANE Select	NP_000079.2:n.1515+19C>G