Canonical Allele Identifier: CA1605823677
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612781_1612785delinsTATTC , CM000668.2:g.1612781_1612785delinsTATTC GRCh38
NC_000006.11:g.1613016_1613020delinsTATTC , CM000668.1:g.1613016_1613020delinsTATTC GRCh37
NC_000006.10:g.1558015_1558019delinsTATTC NCBI36
NG_009368.1:g.7336_7340delinsTATTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*674_*678delinsTATTC MANE Select ENSP00000493906.1:n.*674_*678delinsTATTC
ENST00000380874.3:c.*674_*678delinsTATTC ENSP00000370256.2:n.*674_*678delinsTATTC
NM_001453.2:c.2336_2340delinsTATTC NP_001444.2:n.2336_2340delinsTATTC
NM_001453.3:c.*674_*678delinsTATTC MANE Select NP_001444.2:n.*674_*678delinsTATTC