Canonical Allele Identifier: CA915950616
Gene: COL1A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 804563
ClinVar RCV Id: RCV000991591
dbSNP Id: rs1598297682

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50195944del , CM000679.2:g.50195944del GRCh38
NC_000017.10:g.48273305del , CM000679.1:g.48273305del GRCh37
NC_000017.9:g.45628304del NCBI36
NG_007400.1:g.10698del , LRG_1:g.10698del

Transcript Alleles

HGVS Amino-acid change
ENST00000225964.10:c.1037del MANE Select ENSP00000225964.6:p.Pro346LeufsTer?
ENST00000225964.9:c.1037del ENSP00000225964.5:p.Pro346LeufsTer?
NM_000088.3:c.1037del , LRG_1t1:c.1037del NP_000079.2:p.Pro346LeufsTer?
XM_005257058.3:c.1037del XP_005257115.2:p.Pro346LeufsTer?
XM_005257059.3:c.957+372del XP_005257116.2:n.957+372del
XM_011524341.1:c.957+372del XP_011522643.1:n.957+372del
XM_005257058.4:c.1037del XP_005257115.2:p.Pro346LeufsTer?
XM_005257059.4:c.957+372del XP_005257116.2:n.957+372del
NM_000088.4:c.1037del MANE Select NP_000079.2:p.Pro346LeufsTer?