Canonical Allele Identifier: CA1605821951
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1181818597

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610027_1610028insG , CM000668.2:g.1610027_1610028insG GRCh38
NC_000006.11:g.1610262_1610263insG , CM000668.1:g.1610262_1610263insG GRCh37
NC_000006.10:g.1555261_1555262insG NCBI36
NG_009368.1:g.4582_4583insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-419_-418insG MANE Select ENSP00000493906.1:n.-419_-418insG
ENST00000380874.3:c.-419_-418insG ENSP00000370256.2:n.-419_-418insG
NM_001453.3:c.-419_-418insG MANE Select NP_001444.2:n.-419_-418insG