Canonical Allele Identifier: CA2677060333
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610369_1610370insTGGC , CM000668.2:g.1610369_1610370insTGGC GRCh38
NC_000006.11:g.1610604_1610605insTGGC , CM000668.1:g.1610604_1610605insTGGC GRCh37
NC_000006.10:g.1555603_1555604insTGGC NCBI36
NG_009368.1:g.4924_4925insTGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-77_-76insTGGC MANE Select ENSP00000493906.1:n.-77_-76insTGGC
ENST00000380874.3:c.-77_-76insTGGC ENSP00000370256.2:n.-77_-76insTGGC
NM_001453.3:c.-77_-76insTGGC MANE Select NP_001444.2:n.-77_-76insTGGC