Canonical Allele Identifier: CA10604035
Gene: COL1A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 282016
dbSNP Id: rs886042286

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50186887del , CM000679.2:g.50186887del GRCh38
NC_000017.10:g.48264248del , CM000679.1:g.48264248del GRCh37
NC_000017.9:g.45619247del NCBI36
NG_007400.1:g.19753del , LRG_1:g.19753del

Transcript Alleles

HGVS Amino-acid change
ENST00000225964.10:c.3567del MANE Select ENSP00000225964.6:p.Gly1190ValfsTer?
ENST00000225964.9:c.3567del ENSP00000225964.5:p.Gly1190ValfsTer?
ENST00000510710.3:n.236del
NM_000088.3:c.3567del , LRG_1t1:c.3567del NP_000079.2:p.Gly1190ValfsTer?
XM_005257058.3:c.3297del XP_005257115.2:p.Gly1100ValfsTer?
XM_005257059.3:c.2649del XP_005257116.2:p.Gly884ValfsTer?
XM_011524341.1:c.3369del XP_011522643.1:p.Gly1124ValfsTer?
XM_005257058.4:c.3297del XP_005257115.2:p.Gly1100ValfsTer?
XM_005257059.4:c.2649del XP_005257116.2:p.Gly884ValfsTer?
NM_000088.4:c.3567del MANE Select NP_000079.2:p.Gly1190ValfsTer?