Canonical Allele Identifier: CA1605823725
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612859_1612862delinsAATT , CM000668.2:g.1612859_1612862delinsAATT GRCh38
NC_000006.11:g.1613094_1613097delinsAATT , CM000668.1:g.1613094_1613097delinsAATT GRCh37
NC_000006.10:g.1558093_1558096delinsAATT NCBI36
NG_009368.1:g.7414_7417delinsAATT

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.*752_*755delinsAATT MANE Select ENSP00000493906.1:n.*752_*755delinsAATT
ENST00000380874.3:c.*752_*755delinsAATT ENSP00000370256.2:n.*752_*755delinsAATT
NM_001453.2:c.2414_2417delinsAATT NP_001444.2:n.2414_2417delinsAATT
NM_001453.3:c.*752_*755delinsAATT MANE Select NP_001444.2:n.*752_*755delinsAATT