Canonical Allele Identifier: CA1605822277
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1762513922

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610423_1610432del , CM000668.2:g.1610423_1610432del GRCh38
NC_000006.11:g.1610658_1610667del , CM000668.1:g.1610658_1610667del GRCh37
NC_000006.10:g.1555657_1555666del NCBI36
NG_009368.1:g.4978_4987del

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.-23_-14del MANE Select ENSP00000493906.1:n.-23_-14del
ENST00000380874.3:c.-23_-14del ENSP00000370256.2:n.-23_-14del
NM_001453.3:c.-23_-14del MANE Select NP_001444.2:n.-23_-14del