Canonical Allele Identifier: CA1605822051
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610138_1610139delinsTC , CM000668.2:g.1610138_1610139delinsTC GRCh38
NC_000006.11:g.1610373_1610374delinsTC , CM000668.1:g.1610373_1610374delinsTC GRCh37
NC_000006.10:g.1555372_1555373delinsTC NCBI36
NG_009368.1:g.4693_4694delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-308_-307delinsTC MANE Select ENSP00000493906.1:n.-308_-307delinsTC
ENST00000380874.3:c.-308_-307delinsTC ENSP00000370256.2:n.-308_-307delinsTC
NM_001453.3:c.-308_-307delinsTC MANE Select NP_001444.2:n.-308_-307delinsTC