Canonical Allele Identifier: CA1605822479
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610742_1610773delinsCACCCTGAACGGCATCTACCAGTTCATCATGG , CM000668.2:g.1610742_1610773delinsCACCCTGAACGGCATCTACCAGTTCATCATGG GRCh38
NC_000006.11:g.1610977_1611008delinsCACCCTGAACGGCATCTACCAGTTCATCATGG , CM000668.1:g.1610977_1611008delinsCACCCTGAACGGCATCTACCAGTTCATCATGG GRCh37
NC_000006.10:g.1555976_1556007delinsCACCCTGAACGGCATCTACCAGTTCATCATGG NCBI36
NG_009368.1:g.5297_5328delinsCACCCTGAACGGCATCTACCAGTTCATCATGG

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.297_328delinsCACCCTGAACGGCATCTACCAGTTCATCATGG MANE Select ENSP00000493906.1:p.Ile99=
ENST00000380874.3:c.297_328delinsCACCCTGAACGGCATCTACCAGTTCATCATGG ENSP00000370256.2:p.Ile99=
NM_001453.2:c.297_328delinsCACCCTGAACGGCATCTACCAGTTCATCATGG NP_001444.2:p.Ile99=
NM_001453.3:c.297_328delinsCACCCTGAACGGCATCTACCAGTTCATCATGG MANE Select NP_001444.2:p.Ile99=