Canonical Allele Identifier: CA1605821954
Gene: FOXC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610029_1610030delinsCG , CM000668.2:g.1610029_1610030delinsCG GRCh38
NC_000006.11:g.1610264_1610265delinsCG , CM000668.1:g.1610264_1610265delinsCG GRCh37
NC_000006.10:g.1555263_1555264delinsCG NCBI36
NG_009368.1:g.4584_4585delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-417_-416delinsCG MANE Select ENSP00000493906.1:n.-417_-416delinsCG
ENST00000380874.3:c.-417_-416delinsCG ENSP00000370256.2:n.-417_-416delinsCG
NM_001453.3:c.-417_-416delinsCG MANE Select NP_001444.2:n.-417_-416delinsCG