Canonical Allele Identifier: CA2677060446
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1610479-TC-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610482del , CM000668.2:g.1610482del GRCh38
NC_000006.11:g.1610717del , CM000668.1:g.1610717del GRCh37
NC_000006.10:g.1555716del NCBI36
NG_009368.1:g.5037del

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.37del MANE Select ENSP00000493906.1:p.Leu13TrpfsTer?
ENST00000380874.3:c.37del ENSP00000370256.2:p.Leu13TrpfsTer?
NM_001453.2:c.37del NP_001444.2:p.Leu13TrpfsTer?
NM_001453.3:c.37del MANE Select NP_001444.2:p.Leu13TrpfsTer?