Canonical Allele Identifier: CA1085282401
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1762503007
gnomAD v3: 6-1610026-C-CG
gnomAD v4: 6-1610026-C-CG

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610026_1610027insG , CM000668.2:g.1610026_1610027insG GRCh38
NC_000006.11:g.1610261_1610262insG , CM000668.1:g.1610261_1610262insG GRCh37
NC_000006.10:g.1555260_1555261insG NCBI36
NG_009368.1:g.4581_4582insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-420_-419insG MANE Select ENSP00000493906.1:n.-420_-419insG
ENST00000380874.3:c.-420_-419insG ENSP00000370256.2:n.-420_-419insG
NM_001453.3:c.-420_-419insG MANE Select NP_001444.2:n.-420_-419insG