Canonical Allele Identifier: CA2677060343
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610387_1610425del , CM000668.2:g.1610387_1610425del GRCh38
NC_000006.11:g.1610622_1610660del , CM000668.1:g.1610622_1610660del GRCh37
NC_000006.10:g.1555621_1555659del NCBI36
NG_009368.1:g.4942_4980del

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.-59_-21del MANE Select ENSP00000493906.1:n.-59_-21del
ENST00000380874.3:c.-59_-21del ENSP00000370256.2:n.-59_-21del
NM_001453.3:c.-59_-21del MANE Select NP_001444.2:n.-59_-21del