Canonical Allele Identifier: CA1605823514
Gene: FOXC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612449C= , CM000668.2:g.1612449C= GRCh38
NC_000006.11:g.1612684C= , CM000668.1:g.1612684C= GRCh37
NC_000006.10:g.1557683C= NCBI36
NG_009368.1:g.7004C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*342C= MANE Select ENSP00000493906.1:n.*342C=
ENST00000380874.3:c.*342C= ENSP00000370256.2:n.*342C=
NM_001453.2:c.2004C= NP_001444.2:n.2004C=
NM_001453.3:c.*342C= MANE Select NP_001444.2:n.*342C=
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