Canonical Allele Identifier: CA2695205856
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610699dup , CM000668.2:g.1610699dup GRCh38
NC_000006.11:g.1610934dup , CM000668.1:g.1610934dup GRCh37
NC_000006.10:g.1555933dup NCBI36
NG_009368.1:g.5254dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.254dup MANE Select ENSP00000493906.1:p.Leu86AlafsTer?
ENST00000380874.3:c.254dup ENSP00000370256.2:p.Leu86AlafsTer?
NM_001453.2:c.254dup NP_001444.2:p.Leu86AlafsTer?
NM_001453.3:c.254dup MANE Select NP_001444.2:p.Leu86AlafsTer?