Canonical Allele Identifier: CA1605823663
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612759_1612763delinsTTTTC , CM000668.2:g.1612759_1612763delinsTTTTC GRCh38
NC_000006.11:g.1612994_1612998delinsTTTTC , CM000668.1:g.1612994_1612998delinsTTTTC GRCh37
NC_000006.10:g.1557993_1557997delinsTTTTC NCBI36
NG_009368.1:g.7314_7318delinsTTTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*652_*656delinsTTTTC MANE Select ENSP00000493906.1:n.*652_*656delinsTTTTC
ENST00000380874.3:c.*652_*656delinsTTTTC ENSP00000370256.2:n.*652_*656delinsTTTTC
NM_001453.2:c.2314_2318delinsTTTTC NP_001444.2:n.2314_2318delinsTTTTC
NM_001453.3:c.*652_*656delinsTTTTC MANE Select NP_001444.2:n.*652_*656delinsTTTTC