Canonical Allele Identifier: CA500991642

Gene: COL1A1

Linked Data

• MyVariant Identifiers: chr17:g.48263208G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50185847G>T , CM000679.2:g.50185847G>T	GRCh38
NC_000017.10:g.48263208G>T , CM000679.1:g.48263208G>T	GRCh37
NC_000017.9:g.45618207G>T	NCBI36
NG_007400.1:g.20793C>A , LRG_1:g.20793C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.4179C>A MANE Select	ENSP00000225964.6:p.Ser1393=
ENST00000225964.9:c.4179C>A	ENSP00000225964.5:p.Ser1393=
ENST00000510710.3:n.1144C>A
NM_000088.3:c.4179C>A , LRG_1t1:c.4179C>A	NP_000079.2:p.Ser1393=
XM_005257058.3:c.3909C>A	XP_005257115.2:p.Ser1303=
XM_005257059.3:c.3261C>A	XP_005257116.2:p.Ser1087=
XM_011524341.1:c.3981C>A	XP_011522643.1:p.Ser1327=
XM_005257058.4:c.3909C>A	XP_005257115.2:p.Ser1303=
XM_005257059.4:c.3261C>A	XP_005257116.2:p.Ser1087=
NM_000088.4:c.4179C>A MANE Select	NP_000079.2:p.Ser1393=