Canonical Allele Identifier: CA133388942
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs895506711

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610364_1610369dup , CM000668.2:g.1610364_1610369dup GRCh38
NC_000006.11:g.1610599_1610604dup , CM000668.1:g.1610599_1610604dup GRCh37
NC_000006.10:g.1555598_1555603dup NCBI36
NG_009368.1:g.4919_4924dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-82_-77dup MANE Select ENSP00000493906.1:n.-82_-77dup
ENST00000380874.3:c.-82_-77dup ENSP00000370256.2:n.-82_-77dup
NM_001453.3:c.-82_-77dup MANE Select NP_001444.2:n.-82_-77dup