Canonical Allele Identifier: CA1605821962
Gene: FOXC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610033_1610044delinsCTGGTTATTTGG , CM000668.2:g.1610033_1610044delinsCTGGTTATTTGG GRCh38
NC_000006.11:g.1610268_1610279delinsCTGGTTATTTGG , CM000668.1:g.1610268_1610279delinsCTGGTTATTTGG GRCh37
NC_000006.10:g.1555267_1555278delinsCTGGTTATTTGG NCBI36
NG_009368.1:g.4588_4599delinsCTGGTTATTTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-413_-402delinsCTGGTTATTTGG MANE Select ENSP00000493906.1:n.-413_-402delinsCTGGTTATTTGG
ENST00000380874.3:c.-413_-402delinsCTGGTTATTTGG ENSP00000370256.2:n.-413_-402delinsCTGGTTATTTGG
NM_001453.3:c.-413_-402delinsCTGGTTATTTGG MANE Select NP_001444.2:n.-413_-402delinsCTGGTTATTTGG
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