Canonical Allele Identifier: CA1085284773
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1762575055
gnomAD v3: 6-1612482-G-GCCTTCTTCCTTGCCTCTCA
gnomAD v4: 6-1612482-G-GCCTTCTTCCTTGCCTCTCA
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612486_1612504dup , CM000668.2:g.1612486_1612504dup GRCh38
NC_000006.11:g.1612721_1612739dup , CM000668.1:g.1612721_1612739dup GRCh37
NC_000006.10:g.1557720_1557738dup NCBI36
NG_009368.1:g.7041_7059dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*379_*397dup MANE Select ENSP00000493906.1:n.*379_*397dup
ENST00000380874.3:c.*379_*397dup ENSP00000370256.2:n.*379_*397dup
NM_001453.2:c.2041_2059dup NP_001444.2:n.2041_2059dup
NM_001453.3:c.*379_*397dup MANE Select NP_001444.2:n.*379_*397dup
Search 100 bp 5'
Search 100 bp 3'