Canonical Allele Identifier: CA2710886391
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs2113116041
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612468del , CM000668.2:g.1612468del GRCh38
NC_000006.11:g.1612703del , CM000668.1:g.1612703del GRCh37
NC_000006.10:g.1557702del NCBI36
NG_009368.1:g.7023del

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*361del MANE Select ENSP00000493906.1:n.*361del
ENST00000380874.3:c.*361del ENSP00000370256.2:n.*361del
NM_001453.2:c.2023del NP_001444.2:n.2023del
NM_001453.3:c.*361del MANE Select NP_001444.2:n.*361del
Search 100 bp 5'
Search 100 bp 3'