Canonical Allele Identifier: CA2769749153
Gene: FOXC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612536A>C , CM000668.2:g.1612536A>C GRCh38
NC_000006.11:g.1612771A>C , CM000668.1:g.1612771A>C GRCh37
NC_000006.10:g.1557770A>C NCBI36
NG_009368.1:g.7091A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*429A>C MANE Select ENSP00000493906.1:n.*429A>C
ENST00000380874.3:c.*429A>C ENSP00000370256.2:n.*429A>C
NM_001453.2:c.2091A>C NP_001444.2:n.2091A>C
NM_001453.3:c.*429A>C MANE Select NP_001444.2:n.*429A>C
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