Canonical Allele Identifier: CA1085282314
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1762502222
gnomAD v3: 6-1610018-C-CA
gnomAD v4: 6-1610018-C-CA

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610018_1610019insA , CM000668.2:g.1610018_1610019insA GRCh38
NC_000006.11:g.1610253_1610254insA , CM000668.1:g.1610253_1610254insA GRCh37
NC_000006.10:g.1555252_1555253insA NCBI36
NG_009368.1:g.4573_4574insA

Transcript Alleles

HGVS Amino-acid change
ENST00000645831.2:c.-428_-427insA MANE Select ENSP00000493906.1:n.-428_-427insA
ENST00000380874.3:c.-428_-427insA ENSP00000370256.2:n.-428_-427insA
NM_001453.3:c.-428_-427insA MANE Select NP_001444.2:n.-428_-427insA