Canonical Allele Identifier: CA2695198804
Gene: FOXC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2635518
ClinVar RCV Id: RCV003419013

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610549_1610550delinsT , CM000668.2:g.1610549_1610550delinsT GRCh38
NC_000006.11:g.1610784_1610785delinsT , CM000668.1:g.1610784_1610785delinsT GRCh37
NC_000006.10:g.1555783_1555784delinsT NCBI36
NG_009368.1:g.5104_5105delinsT

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.104_105delinsT MANE Select ENSP00000493906.1:p.Gly35ValfsTer10
ENST00000380874.3:c.104_105delinsT ENSP00000370256.2:p.Gly35ValfsTer10
NM_001453.2:c.104_105delinsT NP_001444.2:p.Gly35ValfsTer10
NM_001453.3:c.104_105delinsT MANE Select NP_001444.2:p.Gly35ValfsTer10