Canonical Allele Identifier: CA362558139
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610576T>A , CM000668.2:g.1610576T>A GRCh38
NC_000006.11:g.1610811T>A , CM000668.1:g.1610811T>A GRCh37
NC_000006.10:g.1555810T>A NCBI36
NG_009368.1:g.5131T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.131T>A MANE Select ENSP00000493906.1:p.Met44Lys
ENST00000380874.3:c.131T>A ENSP00000370256.2:p.Met44Lys
NM_001453.2:c.131T>A NP_001444.2:p.Met44Lys
NM_001453.3:c.131T>A MANE Select NP_001444.2:p.Met44Lys