Canonical Allele Identifier: CA1085282121
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v3: 6-1610013-C-CG
gnomAD v4: 6-1610013-C-CG

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610015dup , CM000668.2:g.1610015dup GRCh38
NC_000006.11:g.1610250dup , CM000668.1:g.1610250dup GRCh37
NC_000006.10:g.1555249dup NCBI36
NG_009368.1:g.4570dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-431dup MANE Select ENSP00000493906.1:n.-431dup
ENST00000380874.3:c.-431dup ENSP00000370256.2:n.-431dup
NM_001453.3:c.-431dup MANE Select NP_001444.2:n.-431dup