Canonical Allele Identifier: CA2580074183
Gene: FOXC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2017556
ClinVar RCV Id: RCV002835257

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610549_1610550insT , CM000668.2:g.1610549_1610550insT GRCh38
NC_000006.11:g.1610784_1610785insT , CM000668.1:g.1610784_1610785insT GRCh37
NC_000006.10:g.1555783_1555784insT NCBI36
NG_009368.1:g.5104_5105insT

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.104_105insT MANE Select ENSP00000493906.1:p.Gly36ArgfsTer?
ENST00000380874.3:c.104_105insT ENSP00000370256.2:p.Gly36ArgfsTer?
NM_001453.2:c.104_105insT NP_001444.2:p.Gly36ArgfsTer?
NM_001453.3:c.104_105insT MANE Select NP_001444.2:p.Gly36ArgfsTer?