Canonical Allele Identifier: CA917658575
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1561674103

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610015_1610016insGCCGC , CM000668.2:g.1610015_1610016insGCCGC GRCh38
NC_000006.11:g.1610250_1610251insGCCGC , CM000668.1:g.1610250_1610251insGCCGC GRCh37
NC_000006.10:g.1555249_1555250insGCCGC NCBI36
NG_009368.1:g.4570_4571insGCCGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-431_-430insGCCGC MANE Select ENSP00000493906.1:n.-431_-430insGCCGC
ENST00000380874.3:c.-431_-430insGCCGC ENSP00000370256.2:n.-431_-430insGCCGC
NM_001453.3:c.-431_-430insGCCGC MANE Select NP_001444.2:n.-431_-430insGCCGC