Canonical Allele Identifier: CA2677060985
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612531_1612533del , CM000668.2:g.1612531_1612533del GRCh38
NC_000006.11:g.1612766_1612768del , CM000668.1:g.1612766_1612768del GRCh37
NC_000006.10:g.1557765_1557767del NCBI36
NG_009368.1:g.7086_7088del

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*424_*426del MANE Select ENSP00000493906.1:n.*424_*426del
ENST00000380874.3:c.*424_*426del ENSP00000370256.2:n.*424_*426del
NM_001453.2:c.2086_2088del NP_001444.2:n.2086_2088del
NM_001453.3:c.*424_*426del MANE Select NP_001444.2:n.*424_*426del