Canonical Allele Identifier: CA1085282094
Gene: FOXC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610010_1610012dup , CM000668.2:g.1610010_1610012dup GRCh38
NC_000006.11:g.1610245_1610247dup , CM000668.1:g.1610245_1610247dup GRCh37
NC_000006.10:g.1555244_1555246dup NCBI36
NG_009368.1:g.4565_4567dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-436_-434dup MANE Select ENSP00000493906.1:n.-436_-434dup
ENST00000380874.3:c.-436_-434dup ENSP00000370256.2:n.-436_-434dup
NM_001453.3:c.-436_-434dup MANE Select NP_001444.2:n.-436_-434dup