Canonical Allele Identifier: CA1605821960
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1762503330

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610031_1610035del , CM000668.2:g.1610031_1610035del GRCh38
NC_000006.11:g.1610266_1610270del , CM000668.1:g.1610266_1610270del GRCh37
NC_000006.10:g.1555265_1555269del NCBI36
NG_009368.1:g.4586_4590del

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-415_-411del MANE Select ENSP00000493906.1:n.-415_-411del
ENST00000380874.3:c.-415_-411del ENSP00000370256.2:n.-415_-411del
NM_001453.3:c.-415_-411del MANE Select NP_001444.2:n.-415_-411del