Canonical Allele Identifier: CA1605823710
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612829C= , CM000668.2:g.1612829C= GRCh38
NC_000006.11:g.1613064C= , CM000668.1:g.1613064C= GRCh37
NC_000006.10:g.1558063C= NCBI36
NG_009368.1:g.7384C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*722C= MANE Select ENSP00000493906.1:n.*722C=
ENST00000380874.3:c.*722C= ENSP00000370256.2:n.*722C=
NM_001453.2:c.2384C= NP_001444.2:n.2384C=
NM_001453.3:c.*722C= MANE Select NP_001444.2:n.*722C=