Canonical Allele Identifier: CA821645455

Gene: FOXC1

Linked Data

• dbSNP Id: rs1404978886
• gnomAD v3: 6-1610025-C-CG
• gnomAD v4: 6-1610025-C-CG
• MyVariant Identifiers: chr6:g.1610260_1610261insG (hg19) ; chr6:g.1610025_1610026insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.1610025_1610026insG , CM000668.2:g.1610025_1610026insG	GRCh38
NC_000006.11:g.1610260_1610261insG , CM000668.1:g.1610260_1610261insG	GRCh37
NC_000006.10:g.1555259_1555260insG	NCBI36
NG_009368.1:g.4580_4581insG

Transcript Alleles

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