Canonical Allele Identifier: CA821650286
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1310429500
MyVariant Identifiers: chr6:g.1613402_1613403insTGATT (hg19) chr6:g.1613167_1613168insTGATT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1613171_1613172insTTGAT , CM000668.2:g.1613171_1613172insTTGAT GRCh38
NC_000006.11:g.1613406_1613407insTTGAT , CM000668.1:g.1613406_1613407insTTGAT GRCh37
NC_000006.10:g.1558405_1558406insTTGAT NCBI36
NG_009368.1:g.7726_7727insTTGAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*1064_*1065insTTGAT MANE Select ENSP00000493906.1:n.*1064_*1065insTTGAT
ENST00000380874.3:c.*1064_*1065insTTGAT ENSP00000370256.2:n.*1064_*1065insTTGAT
NM_001453.2:c.2726_2727insTTGAT NP_001444.2:n.2726_2727insTTGAT
NM_001453.3:c.*1064_*1065insTTGAT MANE Select NP_001444.2:n.*1064_*1065insTTGAT
Search 100 bp 5'
Search 100 bp 3'