Canonical Allele Identifier: CA1605822525
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610825G= , CM000668.2:g.1610825G= GRCh38
NC_000006.11:g.1611060G= , CM000668.1:g.1611060G= GRCh37
NC_000006.10:g.1556059G= NCBI36
NG_009368.1:g.5380G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.380G= MANE Select ENSP00000493906.1:p.Arg127=
ENST00000380874.3:c.380G= ENSP00000370256.2:p.Arg127=
NM_001453.2:c.380G= NP_001444.2:p.Arg127=
NM_001453.3:c.380G= MANE Select NP_001444.2:p.Arg127=