Canonical Allele Identifier: CA2677060350
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610388_1610431del , CM000668.2:g.1610388_1610431del GRCh38
NC_000006.11:g.1610623_1610666del , CM000668.1:g.1610623_1610666del GRCh37
NC_000006.10:g.1555622_1555665del NCBI36
NG_009368.1:g.4943_4986del

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.-58_-15del MANE Select ENSP00000493906.1:n.-58_-15del
ENST00000380874.3:c.-58_-15del ENSP00000370256.2:n.-58_-15del
NM_001453.3:c.-58_-15del MANE Select NP_001444.2:n.-58_-15del