Canonical Allele Identifier: CA2769749193
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1613263_1613269del , CM000668.2:g.1613263_1613269del GRCh38
NC_000006.11:g.1613498_1613504del , CM000668.1:g.1613498_1613504del GRCh37
NC_000006.10:g.1558497_1558503del NCBI36
NG_009368.1:g.7818_7824del

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*1156_*1162del MANE Select ENSP00000493906.1:n.*1156_*1162del
ENST00000380874.3:c.*1156_*1162del ENSP00000370256.2:n.*1156_*1162del
NM_001453.2:c.2818_2824del NP_001444.2:n.2818_2824del
NM_001453.3:c.*1156_*1162del MANE Select NP_001444.2:n.*1156_*1162del