Canonical Allele Identifier: CA500991718

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48263262G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50185901G>C , CM000679.2:g.50185901G>C	GRCh38
NC_000017.10:g.48263262G>C , CM000679.1:g.48263262G>C	GRCh37
NC_000017.9:g.45618261G>C	NCBI36
NG_007400.1:g.20739C>G , LRG_1:g.20739C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.4125C>G MANE Select	ENSP00000225964.6:p.Ala1375=
ENST00000225964.9:c.4125C>G	ENSP00000225964.5:p.Ala1375=
ENST00000510710.3:n.1090C>G
NM_000088.3:c.4125C>G , LRG_1t1:c.4125C>G	NP_000079.2:p.Ala1375=
XM_005257058.3:c.3855C>G	XP_005257115.2:p.Ala1285=
XM_005257059.3:c.3207C>G	XP_005257116.2:p.Ala1069=
XM_011524341.1:c.3927C>G	XP_011522643.1:p.Ala1309=
XM_005257058.4:c.3855C>G	XP_005257115.2:p.Ala1285=
XM_005257059.4:c.3207C>G	XP_005257116.2:p.Ala1069=
NM_000088.4:c.4125C>G MANE Select	NP_000079.2:p.Ala1375=