Canonical Allele Identifier: CA1605823892
Gene: FOXC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1613202C= , CM000668.2:g.1613202C= GRCh38
NC_000006.11:g.1613437C= , CM000668.1:g.1613437C= GRCh37
NC_000006.10:g.1558436C= NCBI36
NG_009368.1:g.7757C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*1095C= MANE Select ENSP00000493906.1:n.*1095C=
ENST00000380874.3:c.*1095C= ENSP00000370256.2:n.*1095C=
NM_001453.2:c.2757C= NP_001444.2:n.2757C=
NM_001453.3:c.*1095C= MANE Select NP_001444.2:n.*1095C=
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