Canonical Allele Identifier: CA2677061121
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1612925-GA-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612930del , CM000668.2:g.1612930del GRCh38
NC_000006.11:g.1613165del , CM000668.1:g.1613165del GRCh37
NC_000006.10:g.1558164del NCBI36
NG_009368.1:g.7485del

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*823del MANE Select ENSP00000493906.1:n.*823del
ENST00000380874.3:c.*823del ENSP00000370256.2:n.*823del
NM_001453.2:c.2485del NP_001444.2:n.2485del
NM_001453.3:c.*823del MANE Select NP_001444.2:n.*823del