Canonical Allele Identifier: CA1605822425
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610637C= , CM000668.2:g.1610637C= GRCh38
NC_000006.11:g.1610872C= , CM000668.1:g.1610872C= GRCh37
NC_000006.10:g.1555871C= NCBI36
NG_009368.1:g.5192C=

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.192C= MANE Select ENSP00000493906.1:p.Tyr64=
ENST00000380874.3:c.192C= ENSP00000370256.2:p.Tyr64=
NM_001453.2:c.192C= NP_001444.2:p.Tyr64=
NM_001453.3:c.192C= MANE Select NP_001444.2:p.Tyr64=