Canonical Allele Identifier: CA1605822719
Gene: FOXC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1611169C= , CM000668.2:g.1611169C= GRCh38
NC_000006.11:g.1611404C= , CM000668.1:g.1611404C= GRCh37
NC_000006.10:g.1556403C= NCBI36
NG_009368.1:g.5724C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.724C= MANE Select ENSP00000493906.1:p.Pro242=
ENST00000380874.3:c.724C= ENSP00000370256.2:p.Pro242=
NM_001453.2:c.724C= NP_001444.2:p.Pro242=
NM_001453.3:c.724C= MANE Select NP_001444.2:p.Pro242=
Search 100 bp 5'
Search 100 bp 3'