Canonical Allele Identifier: CA2769749168
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612744_1612745insACA , CM000668.2:g.1612744_1612745insACA GRCh38
NC_000006.11:g.1612979_1612980insACA , CM000668.1:g.1612979_1612980insACA GRCh37
NC_000006.10:g.1557978_1557979insACA NCBI36
NG_009368.1:g.7299_7300insACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*637_*638insACA MANE Select ENSP00000493906.1:n.*637_*638insACA
ENST00000380874.3:c.*637_*638insACA ENSP00000370256.2:n.*637_*638insACA
NM_001453.2:c.2299_2300insACA NP_001444.2:n.2299_2300insACA
NM_001453.3:c.*637_*638insACA MANE Select NP_001444.2:n.*637_*638insACA