Canonical Allele Identifier: CA2769751887
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610019_1610020insGC , CM000668.2:g.1610019_1610020insGC GRCh38
NC_000006.11:g.1610254_1610255insGC , CM000668.1:g.1610254_1610255insGC GRCh37
NC_000006.10:g.1555253_1555254insGC NCBI36
NG_009368.1:g.4574_4575insGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-427_-426insGC MANE Select ENSP00000493906.1:n.-427_-426insGC
ENST00000380874.3:c.-427_-426insGC ENSP00000370256.2:n.-427_-426insGC
NM_001453.3:c.-427_-426insGC MANE Select NP_001444.2:n.-427_-426insGC