Canonical Allele Identifier: CA1605823552
Gene: FOXC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612507A= , CM000668.2:g.1612507A= GRCh38
NC_000006.11:g.1612742A= , CM000668.1:g.1612742A= GRCh37
NC_000006.10:g.1557741A= NCBI36
NG_009368.1:g.7062A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*400A= MANE Select ENSP00000493906.1:n.*400A=
ENST00000380874.3:c.*400A= ENSP00000370256.2:n.*400A=
NM_001453.2:c.2062A= NP_001444.2:n.2062A=
NM_001453.3:c.*400A= MANE Select NP_001444.2:n.*400A=
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