Canonical Allele Identifier: CA2573140135
Gene: FOXC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1685825
ClinVar RCV Id: RCV002249992
dbSNP Id: rs2113111662

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610843_1610846del , CM000668.2:g.1610843_1610846del GRCh38
NC_000006.11:g.1611078_1611081del , CM000668.1:g.1611078_1611081del GRCh37
NC_000006.10:g.1556077_1556080del NCBI36
NG_009368.1:g.5398_5401del

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.398_401del MANE Select ENSP00000493906.1:p.Asn133SerfsTer?
ENST00000380874.3:c.398_401del ENSP00000370256.2:p.Asn133SerfsTer?
NM_001453.2:c.398_401del NP_001444.2:p.Asn133SerfsTer?
NM_001453.3:c.398_401del MANE Select NP_001444.2:p.Asn133SerfsTer?