Canonical Allele Identifier: CA1605823784
Gene: FOXC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612968_1612970delinsTAA , CM000668.2:g.1612968_1612970delinsTAA GRCh38
NC_000006.11:g.1613203_1613205delinsTAA , CM000668.1:g.1613203_1613205delinsTAA GRCh37
NC_000006.10:g.1558202_1558204delinsTAA NCBI36
NG_009368.1:g.7523_7525delinsTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*861_*863delinsTAA MANE Select ENSP00000493906.1:n.*861_*863delinsTAA
ENST00000380874.3:c.*861_*863delinsTAA ENSP00000370256.2:n.*861_*863delinsTAA
NM_001453.2:c.2523_2525delinsTAA NP_001444.2:n.2523_2525delinsTAA
NM_001453.3:c.*861_*863delinsTAA MANE Select NP_001444.2:n.*861_*863delinsTAA
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