Canonical Allele Identifier: CA1085282478
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610033_1610034insCCCCCCCT , CM000668.2:g.1610033_1610034insCCCCCCCT GRCh38
NC_000006.11:g.1610268_1610269insCCCCCCCT , CM000668.1:g.1610268_1610269insCCCCCCCT GRCh37
NC_000006.10:g.1555267_1555268insCCCCCCCT NCBI36
NG_009368.1:g.4588_4589insCCCCCCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-413_-412insCCCCCCCT MANE Select ENSP00000493906.1:n.-413_-412insCCCCCCCT
ENST00000380874.3:c.-413_-412insCCCCCCCT ENSP00000370256.2:n.-413_-412insCCCCCCCT
NM_001453.3:c.-413_-412insCCCCCCCT MANE Select NP_001444.2:n.-413_-412insCCCCCCCT