Canonical Allele Identifier: CA2710886610
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs2113117102
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1613264dup , CM000668.2:g.1613264dup GRCh38
NC_000006.11:g.1613499dup , CM000668.1:g.1613499dup GRCh37
NC_000006.10:g.1558498dup NCBI36
NG_009368.1:g.7819dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*1157dup MANE Select ENSP00000493906.1:n.*1157dup
ENST00000380874.3:c.*1157dup ENSP00000370256.2:n.*1157dup
NM_001453.2:c.2819dup NP_001444.2:n.2819dup
NM_001453.3:c.*1157dup MANE Select NP_001444.2:n.*1157dup
Search 100 bp 5'
Search 100 bp 3'