Canonical Allele Identifier: CA2324927559
Gene: CYP4F22 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.15540682_15540683delinsAC , CM000681.2:g.15540682_15540683delinsAC GRCh38
NC_000019.9:g.15651493_15651494delinsAC , CM000681.1:g.15651493_15651494delinsAC GRCh37
NC_000019.8:g.15512493_15512494delinsAC NCBI36
NG_007987.1:g.37158_37159delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000269703.8:c.904_905delinsAC MANE Select ENSP00000269703.1:p.Thr302=
ENST00000269703.7:c.904_905delinsAC ENSP00000269703.1:p.Thr302=
ENST00000601005.2:c.904_905delinsAC ENSP00000469866.1:p.Thr302=
NM_173483.3:c.904_905delinsAC NP_775754.2:p.Thr302=
XM_011527692.1:c.904_905delinsAC XP_011525994.1:p.Thr302=
XM_011527693.1:c.904_905delinsAC XP_011525995.1:p.Thr302=
XM_011527692.2:c.904_905delinsAC XP_011525994.1:p.Thr302=
XM_011527693.2:c.904_905delinsAC XP_011525995.1:p.Thr302=
NM_173483.4:c.904_905delinsAC MANE Select NP_775754.2:p.Thr302=
Search 100 bp 5'
Search 100 bp 3'