Canonical Allele Identifier: CA1085282114
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1762501605

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610012_1610013insGGGGGGGGGG , CM000668.2:g.1610012_1610013insGGGGGGGGGG GRCh38
NC_000006.11:g.1610247_1610248insGGGGGGGGGG , CM000668.1:g.1610247_1610248insGGGGGGGGGG GRCh37
NC_000006.10:g.1555246_1555247insGGGGGGGGGG NCBI36
NG_009368.1:g.4567_4568insGGGGGGGGGG

Transcript Alleles

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