Canonical Allele Identifier: CA650480770
Gene: FOXC1 HGNC NCBI

Linked Data

COSMIC: COSN21529772
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612944dup , CM000668.2:g.1612944dup GRCh38
NC_000006.11:g.1613179dup , CM000668.1:g.1613179dup GRCh37
NC_000006.10:g.1558178dup NCBI36
NG_009368.1:g.7499dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*837dup MANE Select ENSP00000493906.1:n.*837dup
ENST00000380874.3:c.*837dup ENSP00000370256.2:n.*837dup
NM_001453.2:c.2499dup NP_001444.2:n.2499dup
NM_001453.3:c.*837dup MANE Select NP_001444.2:n.*837dup
Search 100 bp 5'
Search 100 bp 3'