Canonical Allele Identifier: CA821645450
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1297209971
MyVariant Identifiers: chr6:g.1610259_1610260insT (hg19) chr6:g.1610024_1610025insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610024_1610025insT , CM000668.2:g.1610024_1610025insT GRCh38
NC_000006.11:g.1610259_1610260insT , CM000668.1:g.1610259_1610260insT GRCh37
NC_000006.10:g.1555258_1555259insT NCBI36
NG_009368.1:g.4579_4580insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-422_-421insT MANE Select ENSP00000493906.1:n.-422_-421insT
ENST00000380874.3:c.-422_-421insT ENSP00000370256.2:n.-422_-421insT
NM_001453.3:c.-422_-421insT MANE Select NP_001444.2:n.-422_-421insT
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