Canonical Allele Identifier: CA2677060444
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1610454-GC-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610455del , CM000668.2:g.1610455del GRCh38
NC_000006.11:g.1610690del , CM000668.1:g.1610690del GRCh37
NC_000006.10:g.1555689del NCBI36
NG_009368.1:g.5010del

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.10del MANE Select ENSP00000493906.1:p.Arg4AlafsTer?
ENST00000380874.3:c.10del ENSP00000370256.2:p.Arg4AlafsTer?
NM_001453.2:c.10del NP_001444.2:p.Arg4AlafsTer?
NM_001453.3:c.10del MANE Select NP_001444.2:p.Arg4AlafsTer?