Canonical Allele Identifier: CA2677060054
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610012_1610013insGGGGGGGG , CM000668.2:g.1610012_1610013insGGGGGGGG GRCh38
NC_000006.11:g.1610247_1610248insGGGGGGGG , CM000668.1:g.1610247_1610248insGGGGGGGG GRCh37
NC_000006.10:g.1555246_1555247insGGGGGGGG NCBI36
NG_009368.1:g.4567_4568insGGGGGGGG

Transcript Alleles

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