Canonical Allele Identifier: CA1605822063
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1709490285

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610153_1610154insCCACT , CM000668.2:g.1610153_1610154insCCACT GRCh38
NC_000006.11:g.1610388_1610389insCCACT , CM000668.1:g.1610388_1610389insCCACT GRCh37
NC_000006.10:g.1555387_1555388insCCACT NCBI36
NG_009368.1:g.4708_4709insCCACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-293_-292insCCACT MANE Select ENSP00000493906.1:n.-293_-292insCCACT
ENST00000380874.3:c.-293_-292insCCACT ENSP00000370256.2:n.-293_-292insCCACT
NM_001453.3:c.-293_-292insCCACT MANE Select NP_001444.2:n.-293_-292insCCACT