Canonical Allele Identifier: CA1085282209
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs562673925
gnomAD v3: 6-1610015-G-GCCCCC
gnomAD v4: 6-1610015-G-GCCCCC
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610025_1610029dup , CM000668.2:g.1610025_1610029dup GRCh38
NC_000006.11:g.1610260_1610264dup , CM000668.1:g.1610260_1610264dup GRCh37
NC_000006.10:g.1555259_1555263dup NCBI36
NG_009368.1:g.4580_4584dup

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.-421_-417dup MANE Select ENSP00000493906.1:n.-421_-417dup
ENST00000380874.3:c.-421_-417dup ENSP00000370256.2:n.-421_-417dup
NM_001453.3:c.-421_-417dup MANE Select NP_001444.2:n.-421_-417dup
Search 100 bp 5'
Search 100 bp 3'