Canonical Allele Identifier: CA821650136
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1331426200
gnomAD v3: 6-1612803-AAATT-A
gnomAD v4: 6-1612803-AAATT-A
MyVariant Identifiers: chr6:g.1613039_1613042del (hg19) chr6:g.1612804_1612807del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612805_1612808del , CM000668.2:g.1612805_1612808del GRCh38
NC_000006.11:g.1613040_1613043del , CM000668.1:g.1613040_1613043del GRCh37
NC_000006.10:g.1558039_1558042del NCBI36
NG_009368.1:g.7360_7363del

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.*698_*701del MANE Select ENSP00000493906.1:n.*698_*701del
ENST00000380874.3:c.*698_*701del ENSP00000370256.2:n.*698_*701del
NM_001453.2:c.2360_2363del NP_001444.2:n.2360_2363del
NM_001453.3:c.*698_*701del MANE Select NP_001444.2:n.*698_*701del
Search 100 bp 5'
Search 100 bp 3'