Canonical Allele Identifier: CA1605823565
Gene: FOXC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612533G= , CM000668.2:g.1612533G= GRCh38
NC_000006.11:g.1612768G= , CM000668.1:g.1612768G= GRCh37
NC_000006.10:g.1557767G= NCBI36
NG_009368.1:g.7088G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*426G= MANE Select ENSP00000493906.1:n.*426G=
ENST00000380874.3:c.*426G= ENSP00000370256.2:n.*426G=
NM_001453.2:c.2088G= NP_001444.2:n.2088G=
NM_001453.3:c.*426G= MANE Select NP_001444.2:n.*426G=
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