Canonical Allele Identifier: CA1605823568
Gene: FOXC1 HGNC NCBI

Linked Data

dbSNP Id: rs1762575876
gnomAD v4: 6-1612536-A-AG

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1612541dup , CM000668.2:g.1612541dup GRCh38
NC_000006.11:g.1612776dup , CM000668.1:g.1612776dup GRCh37
NC_000006.10:g.1557775dup NCBI36
NG_009368.1:g.7096dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.*434dup MANE Select ENSP00000493906.1:n.*434dup
ENST00000380874.3:c.*434dup ENSP00000370256.2:n.*434dup
NM_001453.2:c.2096dup NP_001444.2:n.2096dup
NM_001453.3:c.*434dup MANE Select NP_001444.2:n.*434dup