Canonical Allele Identifier: CA500992095

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48266789A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50189428A>T , CM000679.2:g.50189428A>T	GRCh38
NC_000017.10:g.48266789A>T , CM000679.1:g.48266789A>T	GRCh37
NC_000017.9:g.45621788A>T	NCBI36
NG_007400.1:g.17212T>A , LRG_1:g.17212T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000225964.10:c.2778T>A MANE Select	ENSP00000225964.6:p.Gly926=
ENST00000225964.9:c.2778T>A	ENSP00000225964.5:p.Gly926=
NM_000088.3:c.2778T>A , LRG_1t1:c.2778T>A	NP_000079.2:p.Gly926=
XM_005257058.3:c.2667+251T>A	XP_005257115.2:n.2667+251T>A
XM_005257059.3:c.1860T>A	XP_005257116.2:p.Gly620=
XM_011524341.1:c.2580T>A	XP_011522643.1:p.Gly860=
XM_005257058.4:c.2667+251T>A	XP_005257115.2:n.2667+251T>A
XM_005257059.4:c.1860T>A	XP_005257116.2:p.Gly620=
NM_000088.4:c.2778T>A MANE Select	NP_000079.2:p.Gly926=