Canonical Allele Identifier: CA1605821946
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1404978886

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610025_1610026insT , CM000668.2:g.1610025_1610026insT GRCh38
NC_000006.11:g.1610260_1610261insT , CM000668.1:g.1610260_1610261insT GRCh37
NC_000006.10:g.1555259_1555260insT NCBI36
NG_009368.1:g.4580_4581insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-421_-420insT MANE Select ENSP00000493906.1:n.-421_-420insT
ENST00000380874.3:c.-421_-420insT ENSP00000370256.2:n.-421_-420insT
NM_001453.3:c.-421_-420insT MANE Select NP_001444.2:n.-421_-420insT