Canonical Allele Identifier: CA2769751880
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610016_1610017insGGGGGGGGGGG , CM000668.2:g.1610016_1610017insGGGGGGGGGGG GRCh38
NC_000006.11:g.1610251_1610252insGGGGGGGGGGG , CM000668.1:g.1610251_1610252insGGGGGGGGGGG GRCh37
NC_000006.10:g.1555250_1555251insGGGGGGGGGGG NCBI36
NG_009368.1:g.4571_4572insGGGGGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-430_-429insGGGGGGGGGGG MANE Select ENSP00000493906.1:n.-430_-429insGGGGGGGGGGG
ENST00000380874.3:c.-430_-429insGGGGGGGGGGG ENSP00000370256.2:n.-430_-429insGGGGGGGGGGG
NM_001453.3:c.-430_-429insGGGGGGGGGGG MANE Select NP_001444.2:n.-430_-429insGGGGGGGGGGG