Canonical Allele Identifier: CA1085282116
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610012_1610013insGGGG , CM000668.2:g.1610012_1610013insGGGG GRCh38
NC_000006.11:g.1610247_1610248insGGGG , CM000668.1:g.1610247_1610248insGGGG GRCh37
NC_000006.10:g.1555246_1555247insGGGG NCBI36
NG_009368.1:g.4567_4568insGGGG

Transcript Alleles

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