Canonical Allele Identifier: CA2677060018
Gene: FOXC1 HGNC NCBI

Linked Data

gnomAD v4: 6-1609951-AGCGGCTGGCGCGCGAGAGACCGAGAAAAGGTGACGCGGGGCCCGGGCAG-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1609957_1610005del , CM000668.2:g.1609957_1610005del GRCh38
NC_000006.11:g.1610192_1610240del , CM000668.1:g.1610192_1610240del GRCh37
NC_000006.10:g.1555191_1555239del NCBI36
NG_009368.1:g.4512_4560del

Transcript Alleles

HGVS Amino-acid Change
ENST00000645831.2:c.-489_-441del MANE Select ENSP00000493906.1:n.-489_-441del
NM_001453.3:c.-489_-441del MANE Select NP_001444.2:n.-489_-441del
Search 100 bp 5'
Search 100 bp 3'