Canonical Allele Identifier: CA1605821866
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609958_1609960delinsGGC , CM000668.2:g.1609958_1609960delinsGGC GRCh38
NC_000006.11:g.1610193_1610195delinsGGC , CM000668.1:g.1610193_1610195delinsGGC GRCh37
NC_000006.10:g.1555192_1555194delinsGGC NCBI36
NG_009368.1:g.4513_4515delinsGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-488_-486delinsGGC MANE Select ENSP00000493906.1:n.-488_-486delinsGGC
NM_001453.3:c.-488_-486delinsGGC MANE Select NP_001444.2:n.-488_-486delinsGGC