Canonical Allele Identifier: CA1605823692
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612799_1612803delinsTAATA , CM000668.2:g.1612799_1612803delinsTAATA GRCh38
NC_000006.11:g.1613034_1613038delinsTAATA , CM000668.1:g.1613034_1613038delinsTAATA GRCh37
NC_000006.10:g.1558033_1558037delinsTAATA NCBI36
NG_009368.1:g.7354_7358delinsTAATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*692_*696delinsTAATA MANE Select ENSP00000493906.1:n.*692_*696delinsTAATA
ENST00000380874.3:c.*692_*696delinsTAATA ENSP00000370256.2:n.*692_*696delinsTAATA
NM_001453.2:c.2354_2358delinsTAATA NP_001444.2:n.2354_2358delinsTAATA
NM_001453.3:c.*692_*696delinsTAATA MANE Select NP_001444.2:n.*692_*696delinsTAATA