Canonical Allele Identifier: CA2677061085
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612839_1612842dup , CM000668.2:g.1612839_1612842dup GRCh38
NC_000006.11:g.1613074_1613077dup , CM000668.1:g.1613074_1613077dup GRCh37
NC_000006.10:g.1558073_1558076dup NCBI36
NG_009368.1:g.7394_7397dup

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.*732_*735dup MANE Select ENSP00000493906.1:n.*732_*735dup
ENST00000380874.3:c.*732_*735dup ENSP00000370256.2:n.*732_*735dup
NM_001453.2:c.2394_2397dup NP_001444.2:n.2394_2397dup
NM_001453.3:c.*732_*735dup MANE Select NP_001444.2:n.*732_*735dup