Canonical Allele Identifier: CA2769751885
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610017_1610018insGGGGGGGGGGGGGGG , CM000668.2:g.1610017_1610018insGGGGGGGGGGGGGGG GRCh38
NC_000006.11:g.1610252_1610253insGGGGGGGGGGGGGGG , CM000668.1:g.1610252_1610253insGGGGGGGGGGGGGGG GRCh37
NC_000006.10:g.1555251_1555252insGGGGGGGGGGGGGGG NCBI36
NG_009368.1:g.4572_4573insGGGGGGGGGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-429_-428insGGGGGGGGGGGGGGG MANE Select ENSP00000493906.1:n.-429_-428insGGGGGGGGGGGGGGG
ENST00000380874.3:c.-429_-428insGGGGGGGGGGGGGGG ENSP00000370256.2:n.-429_-428insGGGGGGGGGGGGGGG
NM_001453.3:c.-429_-428insGGGGGGGGGGGGGGG MANE Select NP_001444.2:n.-429_-428insGGGGGGGGGGGGGGG