Canonical Allele Identifier: CA650480765
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612679_1612680insT , CM000668.2:g.1612679_1612680insT GRCh38
NC_000006.11:g.1612914_1612915insT , CM000668.1:g.1612914_1612915insT GRCh37
NC_000006.10:g.1557913_1557914insT NCBI36
NG_009368.1:g.7234_7235insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*572_*573insT MANE Select ENSP00000493906.1:n.*572_*573insT
ENST00000380874.3:c.*572_*573insT ENSP00000370256.2:n.*572_*573insT
NM_001453.2:c.2234_2235insT NP_001444.2:n.2234_2235insT
NM_001453.3:c.*572_*573insT MANE Select NP_001444.2:n.*572_*573insT