Canonical Allele Identifier: CA2769749192
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1613261del , CM000668.2:g.1613261del GRCh38
NC_000006.11:g.1613496del , CM000668.1:g.1613496del GRCh37
NC_000006.10:g.1558495del NCBI36
NG_009368.1:g.7816del

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*1154del MANE Select ENSP00000493906.1:n.*1154del
ENST00000380874.3:c.*1154del ENSP00000370256.2:n.*1154del
NM_001453.2:c.2816del NP_001444.2:n.2816del
NM_001453.3:c.*1154del MANE Select NP_001444.2:n.*1154del