Canonical Allele Identifier: CA1085282145
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610014_1610015insCCCC , CM000668.2:g.1610014_1610015insCCCC GRCh38
NC_000006.11:g.1610249_1610250insCCCC , CM000668.1:g.1610249_1610250insCCCC GRCh37
NC_000006.10:g.1555248_1555249insCCCC NCBI36
NG_009368.1:g.4569_4570insCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-432_-431insCCCC MANE Select ENSP00000493906.1:n.-432_-431insCCCC
ENST00000380874.3:c.-432_-431insCCCC ENSP00000370256.2:n.-432_-431insCCCC
NM_001453.3:c.-432_-431insCCCC MANE Select NP_001444.2:n.-432_-431insCCCC