Canonical Allele Identifier: CA1085282049
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v3: 6-1609994-CGGGCAGGCGGCCGGCGCGCGG-C
gnomAD v4: 6-1609994-CGGGCAGGCGGCCGGCGCGCGG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609995_1610015del , CM000668.2:g.1609995_1610015del GRCh38
NC_000006.11:g.1610230_1610250del , CM000668.1:g.1610230_1610250del GRCh37
NC_000006.10:g.1555229_1555249del NCBI36
NG_009368.1:g.4550_4570del

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-451_-431del MANE Select ENSP00000493906.1:n.-451_-431del
ENST00000380874.3:c.-451_-431del ENSP00000370256.2:n.-451_-431del
NM_001453.3:c.-451_-431del MANE Select NP_001444.2:n.-451_-431del
Search 100 bp 5'
Search 100 bp 3'