Canonical Allele Identifier: CA2677060396
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610421_1610440del , CM000668.2:g.1610421_1610440del GRCh38
NC_000006.11:g.1610656_1610675del , CM000668.1:g.1610656_1610675del GRCh37
NC_000006.10:g.1555655_1555674del NCBI36
NG_009368.1:g.4976_4995del

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.-25_-6del MANE Select ENSP00000493906.1:n.-25_-6del
ENST00000380874.3:c.-25_-6del ENSP00000370256.2:n.-25_-6del
NM_001453.3:c.-25_-6del MANE Select NP_001444.2:n.-25_-6del