Canonical Allele Identifier: CA1605822551
Gene: FOXC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610886C= , CM000668.2:g.1610886C= GRCh38
NC_000006.11:g.1611121C= , CM000668.1:g.1611121C= GRCh37
NC_000006.10:g.1556120C= NCBI36
NG_009368.1:g.5441C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.441C= MANE Select ENSP00000493906.1:p.Gly147=
ENST00000380874.3:c.441C= ENSP00000370256.2:p.Gly147=
NM_001453.2:c.441C= NP_001444.2:p.Gly147=
NM_001453.3:c.441C= MANE Select NP_001444.2:p.Gly147=
Search 100 bp 5'
Search 100 bp 3'