Canonical Allele Identifier: CA1605823841
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1731113914

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1613092_1613101del , CM000668.2:g.1613092_1613101del GRCh38
NC_000006.11:g.1613327_1613336del , CM000668.1:g.1613327_1613336del GRCh37
NC_000006.10:g.1558326_1558335del NCBI36
NG_009368.1:g.7647_7656del

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*985_*994del MANE Select ENSP00000493906.1:n.*985_*994del
ENST00000380874.3:c.*985_*994del ENSP00000370256.2:n.*985_*994del
NM_001453.2:c.2647_2656del NP_001444.2:n.2647_2656del
NM_001453.3:c.*985_*994del MANE Select NP_001444.2:n.*985_*994del