Canonical Allele Identifier: CA1605823695
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612806T= , CM000668.2:g.1612806T= GRCh38
NC_000006.11:g.1613041T= , CM000668.1:g.1613041T= GRCh37
NC_000006.10:g.1558040T= NCBI36
NG_009368.1:g.7361T=

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.*699T= MANE Select ENSP00000493906.1:n.*699T=
ENST00000380874.3:c.*699T= ENSP00000370256.2:n.*699T=
NM_001453.2:c.2361T= NP_001444.2:n.2361T=
NM_001453.3:c.*699T= MANE Select NP_001444.2:n.*699T=