Canonical Allele Identifier: CA2677060324
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610355_1610375del , CM000668.2:g.1610355_1610375del GRCh38
NC_000006.11:g.1610590_1610610del , CM000668.1:g.1610590_1610610del GRCh37
NC_000006.10:g.1555589_1555609del NCBI36
NG_009368.1:g.4910_4930del

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-91_-71del MANE Select ENSP00000493906.1:n.-91_-71del
ENST00000380874.3:c.-91_-71del ENSP00000370256.2:n.-91_-71del
NM_001453.3:c.-91_-71del MANE Select NP_001444.2:n.-91_-71del