Canonical Allele Identifier: CA362558761
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610857A>C , CM000668.2:g.1610857A>C GRCh38
NC_000006.11:g.1611092A>C , CM000668.1:g.1611092A>C GRCh37
NC_000006.10:g.1556091A>C NCBI36
NG_009368.1:g.5412A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.412A>C MANE Select ENSP00000493906.1:p.Lys138Gln
ENST00000380874.3:c.412A>C ENSP00000370256.2:p.Lys138Gln
NM_001453.2:c.412A>C NP_001444.2:p.Lys138Gln
NM_001453.3:c.412A>C MANE Select NP_001444.2:p.Lys138Gln