Canonical Allele Identifier: CA2677060057
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610024_1610029del , CM000668.2:g.1610024_1610029del GRCh38
NC_000006.11:g.1610259_1610264del , CM000668.1:g.1610259_1610264del GRCh37
NC_000006.10:g.1555258_1555263del NCBI36
NG_009368.1:g.4579_4584del

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.-422_-417del MANE Select ENSP00000493906.1:n.-422_-417del
ENST00000380874.3:c.-422_-417del ENSP00000370256.2:n.-422_-417del
NM_001453.3:c.-422_-417del MANE Select NP_001444.2:n.-422_-417del