Canonical Allele Identifier: CA1605823697
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612808A= , CM000668.2:g.1612808A= GRCh38
NC_000006.11:g.1613043A= , CM000668.1:g.1613043A= GRCh37
NC_000006.10:g.1558042A= NCBI36
NG_009368.1:g.7363A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*701A= MANE Select ENSP00000493906.1:n.*701A=
ENST00000380874.3:c.*701A= ENSP00000370256.2:n.*701A=
NM_001453.2:c.2363A= NP_001444.2:n.2363A=
NM_001453.3:c.*701A= MANE Select NP_001444.2:n.*701A=