Canonical Allele Identifier: CA1605821902
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609994_1609995delinsCG , CM000668.2:g.1609994_1609995delinsCG GRCh38
NC_000006.11:g.1610229_1610230delinsCG , CM000668.1:g.1610229_1610230delinsCG GRCh37
NC_000006.10:g.1555228_1555229delinsCG NCBI36
NG_009368.1:g.4549_4550delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-452_-451delinsCG MANE Select ENSP00000493906.1:n.-452_-451delinsCG
ENST00000380874.3:c.-452_-451delinsCG ENSP00000370256.2:n.-452_-451delinsCG
NM_001453.3:c.-452_-451delinsCG MANE Select NP_001444.2:n.-452_-451delinsCG