Canonical Allele Identifier: CA2769749188
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1613224_1613263del , CM000668.2:g.1613224_1613263del GRCh38
NC_000006.11:g.1613459_1613498del , CM000668.1:g.1613459_1613498del GRCh37
NC_000006.10:g.1558458_1558497del NCBI36
NG_009368.1:g.7779_7818del

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*1117_*1156del MANE Select ENSP00000493906.1:n.*1117_*1156del
ENST00000380874.3:c.*1117_*1156del ENSP00000370256.2:n.*1117_*1156del
NM_001453.2:c.2779_2818del NP_001444.2:n.2779_2818del
NM_001453.3:c.*1117_*1156del MANE Select NP_001444.2:n.*1117_*1156del