Canonical Allele Identifier: CA1605822427
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610639G= , CM000668.2:g.1610639G= GRCh38
NC_000006.11:g.1610874G= , CM000668.1:g.1610874G= GRCh37
NC_000006.10:g.1555873G= NCBI36
NG_009368.1:g.5194G=

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.194G= MANE Select ENSP00000493906.1:p.Gly65=
ENST00000380874.3:c.194G= ENSP00000370256.2:p.Gly65=
NM_001453.2:c.194G= NP_001444.2:p.Gly65=
NM_001453.3:c.194G= MANE Select NP_001444.2:p.Gly65=