Canonical Allele Identifier: CA2839926261
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1611102del , CM000668.2:g.1611102del GRCh38
NC_000006.11:g.1611337del , CM000668.1:g.1611337del GRCh37
NC_000006.10:g.1556336del NCBI36
NG_009368.1:g.5657del

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.657del MANE Select ENSP00000493906.1:p.Val221CysfsTer?
ENST00000380874.3:c.657del ENSP00000370256.2:p.Val221CysfsTer?
NM_001453.2:c.657del NP_001444.2:p.Val221CysfsTer?
NM_001453.3:c.657del MANE Select NP_001444.2:p.Val221CysfsTer?