Canonical Allele Identifier: CA1605823734
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612871A= , CM000668.2:g.1612871A= GRCh38
NC_000006.11:g.1613106A= , CM000668.1:g.1613106A= GRCh37
NC_000006.10:g.1558105A= NCBI36
NG_009368.1:g.7426A=

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.*764A= MANE Select ENSP00000493906.1:n.*764A=
ENST00000380874.3:c.*764A= ENSP00000370256.2:n.*764A=
NM_001453.2:c.2426A= NP_001444.2:n.2426A=
NM_001453.3:c.*764A= MANE Select NP_001444.2:n.*764A=