Canonical Allele Identifier: CA821645467

Gene: FOXC1

Linked Data

• dbSNP Id: rs1358271591
• gnomAD v3: 6-1610029-C-CT
• gnomAD v4: 6-1610029-C-CT
• MyVariant Identifiers: chr6:g.1610264_1610265insT (hg19) ; chr6:g.1610029_1610030insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.1610029_1610030insT , CM000668.2:g.1610029_1610030insT	GRCh38
NC_000006.11:g.1610264_1610265insT , CM000668.1:g.1610264_1610265insT	GRCh37
NC_000006.10:g.1555263_1555264insT	NCBI36
NG_009368.1:g.4584_4585insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645831.2:c.-417_-416insT MANE Select	ENSP00000493906.1:n.-417_-416insT
ENST00000380874.3:c.-417_-416insT	ENSP00000370256.2:n.-417_-416insT
NM_001453.3:c.-417_-416insT MANE Select	NP_001444.2:n.-417_-416insT