Canonical Allele Identifier: CA2546597180
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612732A>C , CM000668.2:g.1612732A>C GRCh38
NC_000006.11:g.1612967A>C , CM000668.1:g.1612967A>C GRCh37
NC_000006.10:g.1557966A>C NCBI36
NG_009368.1:g.7287A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*625A>C MANE Select ENSP00000493906.1:n.*625A>C
ENST00000380874.3:c.*625A>C ENSP00000370256.2:n.*625A>C
NM_001453.2:c.2287A>C NP_001444.2:n.2287A>C
NM_001453.3:c.*625A>C MANE Select NP_001444.2:n.*625A>C