Canonical Allele Identifier: CA1605823676
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612779C= , CM000668.2:g.1612779C= GRCh38
NC_000006.11:g.1613014C= , CM000668.1:g.1613014C= GRCh37
NC_000006.10:g.1558013C= NCBI36
NG_009368.1:g.7334C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*672C= MANE Select ENSP00000493906.1:n.*672C=
ENST00000380874.3:c.*672C= ENSP00000370256.2:n.*672C=
NM_001453.2:c.2334C= NP_001444.2:n.2334C=
NM_001453.3:c.*672C= MANE Select NP_001444.2:n.*672C=