Canonical Allele Identifier: CA916082800
Gene: FOXC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 861432
ClinVar RCV Id: RCV001067954
dbSNP Id: rs1762521548

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610746_1610776del , CM000668.2:g.1610746_1610776del GRCh38
NC_000006.11:g.1610981_1611011del , CM000668.1:g.1610981_1611011del GRCh37
NC_000006.10:g.1555980_1556010del NCBI36
NG_009368.1:g.5301_5331del

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.301_331del MANE Select ENSP00000493906.1:p.Leu101AlafsTer?
ENST00000380874.3:c.301_331del ENSP00000370256.2:p.Leu101AlafsTer?
NM_001453.2:c.301_331del NP_001444.2:p.Leu101AlafsTer?
NM_001453.3:c.301_331del MANE Select NP_001444.2:p.Leu101AlafsTer?