Canonical Allele Identifier: CA400205607

Gene: COL1A1

Linked Data

• gnomAD v4: 17-50189423-G-C
• MyVariant Identifiers: chr17:g.48266784G>C (hg19) ; chr17:g.50189423G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50189423G>C , CM000679.2:g.50189423G>C	GRCh38
NC_000017.10:g.48266784G>C , CM000679.1:g.48266784G>C	GRCh37
NC_000017.9:g.45621783G>C	NCBI36
NG_007400.1:g.17217C>G , LRG_1:g.17217C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000225964.10:c.2783C>G MANE Select	ENSP00000225964.6:p.Pro928Arg
ENST00000225964.9:c.2783C>G	ENSP00000225964.5:p.Pro928Arg
NM_000088.3:c.2783C>G , LRG_1t1:c.2783C>G	NP_000079.2:p.Pro928Arg
XM_005257058.3:c.2667+256C>G	XP_005257115.2:n.2667+256C>G
XM_005257059.3:c.1865C>G	XP_005257116.2:p.Pro622Arg
XM_011524341.1:c.2585C>G	XP_011522643.1:p.Pro862Arg
XM_005257058.4:c.2667+256C>G	XP_005257115.2:n.2667+256C>G
XM_005257059.4:c.1865C>G	XP_005257116.2:p.Pro622Arg
NM_000088.4:c.2783C>G MANE Select	NP_000079.2:p.Pro928Arg