Canonical Allele Identifier: CA1605823706
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612818_1612822delinsTTGAA , CM000668.2:g.1612818_1612822delinsTTGAA GRCh38
NC_000006.11:g.1613053_1613057delinsTTGAA , CM000668.1:g.1613053_1613057delinsTTGAA GRCh37
NC_000006.10:g.1558052_1558056delinsTTGAA NCBI36
NG_009368.1:g.7373_7377delinsTTGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*711_*715delinsTTGAA MANE Select ENSP00000493906.1:n.*711_*715delinsTTGAA
ENST00000380874.3:c.*711_*715delinsTTGAA ENSP00000370256.2:n.*711_*715delinsTTGAA
NM_001453.2:c.2373_2377delinsTTGAA NP_001444.2:n.2373_2377delinsTTGAA
NM_001453.3:c.*711_*715delinsTTGAA MANE Select NP_001444.2:n.*711_*715delinsTTGAA