Canonical Allele Identifier: CA1605823569
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612539G= , CM000668.2:g.1612539G= GRCh38
NC_000006.11:g.1612774G= , CM000668.1:g.1612774G= GRCh37
NC_000006.10:g.1557773G= NCBI36
NG_009368.1:g.7094G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*432G= MANE Select ENSP00000493906.1:n.*432G=
ENST00000380874.3:c.*432G= ENSP00000370256.2:n.*432G=
NM_001453.2:c.2094G= NP_001444.2:n.2094G=
NM_001453.3:c.*432G= MANE Select NP_001444.2:n.*432G=