Canonical Allele Identifier: CA1605823655
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612753A= , CM000668.2:g.1612753A= GRCh38
NC_000006.11:g.1612988A= , CM000668.1:g.1612988A= GRCh37
NC_000006.10:g.1557987A= NCBI36
NG_009368.1:g.7308A=

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.*646A= MANE Select ENSP00000493906.1:n.*646A=
ENST00000380874.3:c.*646A= ENSP00000370256.2:n.*646A=
NM_001453.2:c.2308A= NP_001444.2:n.2308A=
NM_001453.3:c.*646A= MANE Select NP_001444.2:n.*646A=