Canonical Allele Identifier: CA1605823516
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612453_1612454delinsCT , CM000668.2:g.1612453_1612454delinsCT GRCh38
NC_000006.11:g.1612688_1612689delinsCT , CM000668.1:g.1612688_1612689delinsCT GRCh37
NC_000006.10:g.1557687_1557688delinsCT NCBI36
NG_009368.1:g.7008_7009delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*346_*347delinsCT MANE Select ENSP00000493906.1:n.*346_*347delinsCT
ENST00000380874.3:c.*346_*347delinsCT ENSP00000370256.2:n.*346_*347delinsCT
NM_001453.2:c.2008_2009delinsCT NP_001444.2:n.2008_2009delinsCT
NM_001453.3:c.*346_*347delinsCT MANE Select NP_001444.2:n.*346_*347delinsCT