Canonical Allele Identifier: CA1605822466
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610724C= , CM000668.2:g.1610724C= GRCh38
NC_000006.11:g.1610959C= , CM000668.1:g.1610959C= GRCh37
NC_000006.10:g.1555958C= NCBI36
NG_009368.1:g.5279C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.279C= MANE Select ENSP00000493906.1:p.Asn93=
ENST00000380874.3:c.279C= ENSP00000370256.2:p.Asn93=
NM_001453.2:c.279C= NP_001444.2:p.Asn93=
NM_001453.3:c.279C= MANE Select NP_001444.2:p.Asn93=