Canonical Allele Identifier: CA2677060060
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610026_1610033del , CM000668.2:g.1610026_1610033del GRCh38
NC_000006.11:g.1610261_1610268del , CM000668.1:g.1610261_1610268del GRCh37
NC_000006.10:g.1555260_1555267del NCBI36
NG_009368.1:g.4581_4588del

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-420_-413del MANE Select ENSP00000493906.1:n.-420_-413del
ENST00000380874.3:c.-420_-413del ENSP00000370256.2:n.-420_-413del
NM_001453.3:c.-420_-413del MANE Select NP_001444.2:n.-420_-413del