Canonical Allele Identifier: CA1605823721
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612852G= , CM000668.2:g.1612852G= GRCh38
NC_000006.11:g.1613087G= , CM000668.1:g.1613087G= GRCh37
NC_000006.10:g.1558086G= NCBI36
NG_009368.1:g.7407G=

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.*745G= MANE Select ENSP00000493906.1:n.*745G=
ENST00000380874.3:c.*745G= ENSP00000370256.2:n.*745G=
NM_001453.2:c.2407G= NP_001444.2:n.2407G=
NM_001453.3:c.*745G= MANE Select NP_001444.2:n.*745G=