Canonical Allele Identifier: CA650480779
Gene: FOXC1 HGNC NCBI

Linked Data

COSMIC: COSN24301808
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1613202_1613203insT , CM000668.2:g.1613202_1613203insT GRCh38
NC_000006.11:g.1613437_1613438insT , CM000668.1:g.1613437_1613438insT GRCh37
NC_000006.10:g.1558436_1558437insT NCBI36
NG_009368.1:g.7757_7758insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*1095_*1096insT MANE Select ENSP00000493906.1:n.*1095_*1096insT
ENST00000380874.3:c.*1095_*1096insT ENSP00000370256.2:n.*1095_*1096insT
NM_001453.2:c.2757_2758insT NP_001444.2:n.2757_2758insT
NM_001453.3:c.*1095_*1096insT MANE Select NP_001444.2:n.*1095_*1096insT
Search 100 bp 5'
Search 100 bp 3'