Canonical Allele Identifier: CA1605823542
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612501_1612502delinsAC , CM000668.2:g.1612501_1612502delinsAC GRCh38
NC_000006.11:g.1612736_1612737delinsAC , CM000668.1:g.1612736_1612737delinsAC GRCh37
NC_000006.10:g.1557735_1557736delinsAC NCBI36
NG_009368.1:g.7056_7057delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*394_*395delinsAC MANE Select ENSP00000493906.1:n.*394_*395delinsAC
ENST00000380874.3:c.*394_*395delinsAC ENSP00000370256.2:n.*394_*395delinsAC
NM_001453.2:c.2056_2057delinsAC NP_001444.2:n.2056_2057delinsAC
NM_001453.3:c.*394_*395delinsAC MANE Select NP_001444.2:n.*394_*395delinsAC