Canonical Allele Identifier: CA10603279
Gene: FOXC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86568323dup , CM000678.2:g.86568323dup GRCh38
NC_000016.9:g.86601929dup , CM000678.1:g.86601929dup GRCh37
NC_000016.8:g.85159430dup NCBI36
NG_012025.1:g.6073dup
NG_012025.2:g.6495dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000649859.1:c.988dup MANE Select ENSP00000497759.1:p.Gln330ProfsTer?
ENST00000320354.5:c.988dup ENSP00000326371.4:p.Gln330ProfsTer?
NM_005251.2:c.988dup NP_005242.1:p.Gln330ProfsTer?
NM_005251.3:c.988dup MANE Select NP_005242.1:p.Gln330ProfsTer?