Canonical Allele Identifier: CA1147243049
Gene: FOXC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1698748
ClinVar RCV Id: RCV002272605
dbSNP Id: rs2113110837

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610544_1610553del , CM000668.2:g.1610544_1610553del GRCh38
NC_000006.11:g.1610779_1610788del , CM000668.1:g.1610779_1610788del GRCh37
NC_000006.10:g.1555778_1555787del NCBI36
NG_009368.1:g.5099_5108del

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.99_108del MANE Select ENSP00000493906.1:p.Gly34ThrfsTer8
ENST00000380874.3:c.99_108del ENSP00000370256.2:p.Gly34ThrfsTer8
NM_001453.2:c.99_108del NP_001444.2:p.Gly34ThrfsTer8
NM_001453.3:c.99_108del MANE Select NP_001444.2:p.Gly34ThrfsTer8