Canonical Allele Identifier: CA2769751851

Gene: FOXC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.1610012_1610013insGGGGGGGGGGGGGGGGGGGGGGGGG , CM000668.2:g.1610012_1610013insGGGGGGGGGGGGGGGGGGGGGGGGG	GRCh38
NC_000006.11:g.1610247_1610248insGGGGGGGGGGGGGGGGGGGGGGGGG , CM000668.1:g.1610247_1610248insGGGGGGGGGGGGGGGGGGGGGGGGG	GRCh37
NC_000006.10:g.1555246_1555247insGGGGGGGGGGGGGGGGGGGGGGGGG	NCBI36
NG_009368.1:g.4567_4568insGGGGGGGGGGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645831.2:c.-434_-433insGGGGGGGGGGGGGGGGGGGGGGGGG MANE Select	ENSP00000493906.1:n.-434_-433insGGGGGGGGGGGGGGGGGGGGGGGGG
ENST00000380874.3:c.-434_-433insGGGGGGGGGGGGGGGGGGGGGGGGG	ENSP00000370256.2:n.-434_-433insGGGGGGGGGGGGGGGGGGGGGGGGG
NM_001453.3:c.-434_-433insGGGGGGGGGGGGGGGGGGGGGGGGG MANE Select	NP_001444.2:n.-434_-433insGGGGGGGGGGGGGGGGGGGGGGGGG