Canonical Allele Identifier: CA2677061260
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1613267-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1613270del , CM000668.2:g.1613270del GRCh38
NC_000006.11:g.1613505del , CM000668.1:g.1613505del GRCh37
NC_000006.10:g.1558504del NCBI36
NG_009368.1:g.7825del

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*1163del MANE Select ENSP00000493906.1:n.*1163del
ENST00000380874.3:c.*1163del ENSP00000370256.2:n.*1163del
NM_001453.2:c.2825del NP_001444.2:n.2825del
NM_001453.3:c.*1163del MANE Select NP_001444.2:n.*1163del
Search 100 bp 5'
Search 100 bp 3'