Canonical Allele Identifier: CA1605823698
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612809C= , CM000668.2:g.1612809C= GRCh38
NC_000006.11:g.1613044C= , CM000668.1:g.1613044C= GRCh37
NC_000006.10:g.1558043C= NCBI36
NG_009368.1:g.7364C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*702C= MANE Select ENSP00000493906.1:n.*702C=
ENST00000380874.3:c.*702C= ENSP00000370256.2:n.*702C=
NM_001453.2:c.2364C= NP_001444.2:n.2364C=
NM_001453.3:c.*702C= MANE Select NP_001444.2:n.*702C=