Canonical Allele Identifier: CA2677061076
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612805_1612806insCTGTC , CM000668.2:g.1612805_1612806insCTGTC GRCh38
NC_000006.11:g.1613040_1613041insCTGTC , CM000668.1:g.1613040_1613041insCTGTC GRCh37
NC_000006.10:g.1558039_1558040insCTGTC NCBI36
NG_009368.1:g.7360_7361insCTGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*698_*699insCTGTC MANE Select ENSP00000493906.1:n.*698_*699insCTGTC
ENST00000380874.3:c.*698_*699insCTGTC ENSP00000370256.2:n.*698_*699insCTGTC
NM_001453.2:c.2360_2361insCTGTC NP_001444.2:n.2360_2361insCTGTC
NM_001453.3:c.*698_*699insCTGTC MANE Select NP_001444.2:n.*698_*699insCTGTC