Canonical Allele Identifier: CA1605823670
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612765_1612767delinsTTC , CM000668.2:g.1612765_1612767delinsTTC GRCh38
NC_000006.11:g.1613000_1613002delinsTTC , CM000668.1:g.1613000_1613002delinsTTC GRCh37
NC_000006.10:g.1557999_1558001delinsTTC NCBI36
NG_009368.1:g.7320_7322delinsTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*658_*660delinsTTC MANE Select ENSP00000493906.1:n.*658_*660delinsTTC
ENST00000380874.3:c.*658_*660delinsTTC ENSP00000370256.2:n.*658_*660delinsTTC
NM_001453.2:c.2320_2322delinsTTC NP_001444.2:n.2320_2322delinsTTC
NM_001453.3:c.*658_*660delinsTTC MANE Select NP_001444.2:n.*658_*660delinsTTC