Canonical Allele Identifier: CA1139665704

Gene: COL1A1

Linked Data

• ClinVar Variation Id: 933331
• ClinVar RCV Id: RCV001201519
• dbSNP Id: rs1907332311

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50193992_50193999del , CM000679.2:g.50193992_50193999del	GRCh38
NC_000017.10:g.48271353_48271360del , CM000679.1:g.48271353_48271360del	GRCh37
NC_000017.9:g.45626352_45626359del	NCBI36
NG_007400.1:g.12643_12650del , LRG_1:g.12643_12650del

Transcript Alleles

HGVS	Amino-acid change
ENST00000225964.10:c.1713_1720del MANE Select	ENSP00000225964.6:p.Gly572TrpfsTer12
ENST00000225964.9:c.1713_1720del	ENSP00000225964.5:p.Gly572TrpfsTer12
ENST00000463440.1:n.103_110del
ENST00000471344.1:n.745_752del
ENST00000476387.1:n.62_69del
NM_000088.3:c.1713_1720del , LRG_1t1:c.1713_1720del	NP_000079.2:p.Gly572TrpfsTer12
XM_005257058.3:c.1713_1720del	XP_005257115.2:p.Gly572TrpfsTer12
XM_005257059.3:c.958-1304_958-1297del	XP_005257116.2:n.958-1304_958-1297del
XM_011524341.1:c.1515_1522del	XP_011522643.1:p.Gly506TrpfsTer12
XM_005257058.4:c.1713_1720del	XP_005257115.2:p.Gly572TrpfsTer12
XM_005257059.4:c.958-1304_958-1297del	XP_005257116.2:n.958-1304_958-1297del
NM_000088.4:c.1713_1720del MANE Select	NP_000079.2:p.Gly572TrpfsTer12