Canonical Allele Identifier: CA1085282540
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610045_1610046dup , CM000668.2:g.1610045_1610046dup GRCh38
NC_000006.11:g.1610280_1610281dup , CM000668.1:g.1610280_1610281dup GRCh37
NC_000006.10:g.1555279_1555280dup NCBI36
NG_009368.1:g.4600_4601dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-401_-400dup MANE Select ENSP00000493906.1:n.-401_-400dup
ENST00000380874.3:c.-401_-400dup ENSP00000370256.2:n.-401_-400dup
NM_001453.3:c.-401_-400dup MANE Select NP_001444.2:n.-401_-400dup