Canonical Allele Identifier: CA2583107940
Gene: CYP4F22 HGNC NCBI

Linked Data

gnomAD v4: 19-15540336-AG-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540339del , CM000681.2:g.15540339del GRCh38
NC_000019.9:g.15651150del , CM000681.1:g.15651150del GRCh37
NC_000019.8:g.15512150del NCBI36
NG_007987.1:g.36815del

Transcript Alleles

HGVS Amino-acid change
ENST00000269703.8:c.672-111del MANE Select ENSP00000269703.1:n.672-111del
ENST00000269703.7:c.672-111del ENSP00000269703.1:n.672-111del
ENST00000601005.2:c.672-111del ENSP00000469866.1:n.672-111del
NM_173483.3:c.672-111del NP_775754.2:n.672-111del
XM_011527692.1:c.672-111del XP_011525994.1:n.672-111del
XM_011527693.1:c.672-111del XP_011525995.1:n.672-111del
XM_011527692.2:c.672-111del XP_011525994.1:n.672-111del
XM_011527693.2:c.672-111del XP_011525995.1:n.672-111del
NM_173483.4:c.672-111del MANE Select NP_775754.2:n.672-111del
Search 100 bp 5'
Search 100 bp 3'