Canonical Allele Identifier: CA2590755713
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610015_1610016insGGGGGGGGGGGGG , CM000668.2:g.1610015_1610016insGGGGGGGGGGGGG GRCh38
NC_000006.11:g.1610250_1610251insGGGGGGGGGGGGG , CM000668.1:g.1610250_1610251insGGGGGGGGGGGGG GRCh37
NC_000006.10:g.1555249_1555250insGGGGGGGGGGGGG NCBI36
NG_009368.1:g.4570_4571insGGGGGGGGGGGGG

Transcript Alleles

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