Canonical Allele Identifier: CA2769751863
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610015_1610016insGGGGGGGGGGGGGGGG , CM000668.2:g.1610015_1610016insGGGGGGGGGGGGGGGG GRCh38
NC_000006.11:g.1610250_1610251insGGGGGGGGGGGGGGGG , CM000668.1:g.1610250_1610251insGGGGGGGGGGGGGGGG GRCh37
NC_000006.10:g.1555249_1555250insGGGGGGGGGGGGGGGG NCBI36
NG_009368.1:g.4570_4571insGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-431_-430insGGGGGGGGGGGGGGGG MANE Select ENSP00000493906.1:n.-431_-430insGGGGGGGGGGGGGGGG
ENST00000380874.3:c.-431_-430insGGGGGGGGGGGGGGGG ENSP00000370256.2:n.-431_-430insGGGGGGGGGGGGGGGG
NM_001453.3:c.-431_-430insGGGGGGGGGGGGGGGG MANE Select NP_001444.2:n.-431_-430insGGGGGGGGGGGGGGGG