Canonical Allele Identifier: CA1605823567
Gene: FOXC1 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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