Canonical Allele Identifier: CA2677060163
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1610194-GC-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1610196del , CM000668.2:g.1610196del GRCh38
NC_000006.11:g.1610431del , CM000668.1:g.1610431del GRCh37
NC_000006.10:g.1555430del NCBI36
NG_009368.1:g.4751del

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-250del MANE Select ENSP00000493906.1:n.-250del
ENST00000380874.3:c.-250del ENSP00000370256.2:n.-250del
NM_001453.3:c.-250del MANE Select NP_001444.2:n.-250del