Canonical Allele Identifier: CA1605823602
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612631T= , CM000668.2:g.1612631T= GRCh38
NC_000006.11:g.1612866T= , CM000668.1:g.1612866T= GRCh37
NC_000006.10:g.1557865T= NCBI36
NG_009368.1:g.7186T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*524T= MANE Select ENSP00000493906.1:n.*524T=
ENST00000380874.3:c.*524T= ENSP00000370256.2:n.*524T=
NM_001453.2:c.2186T= NP_001444.2:n.2186T=
NM_001453.3:c.*524T= MANE Select NP_001444.2:n.*524T=