Canonical Allele Identifier: CA565356178

Gene: FOXC1

Linked Data

• dbSNP Id: rs1192019316
• gnomAD v2: 6-1610641-GGGGGCGGCGGGCGGCGC-G
• gnomAD v4: 6-1610406-GGGGGCGGCGGGCGGCGC-G
• MyVariant Identifiers: chr6:g.1610642_1610658del (hg19) ; chr6:g.1610407_1610423del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.1610417_1610433del , CM000668.2:g.1610417_1610433del	GRCh38
NC_000006.11:g.1610652_1610668del , CM000668.1:g.1610652_1610668del	GRCh37
NC_000006.10:g.1555651_1555667del	NCBI36
NG_009368.1:g.4972_4988del

Transcript Alleles

HGVS	Amino-acid change
ENST00000645831.2:c.-29_-13del MANE Select	ENSP00000493906.1:n.-29_-13del
ENST00000380874.3:c.-29_-13del	ENSP00000370256.2:n.-29_-13del
NM_001453.3:c.-29_-13del MANE Select	NP_001444.2:n.-29_-13del