Canonical Allele Identifier: CA2576657820

Gene: CYP4F22

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.904del MANE Select	ENSP00000269703.1:p.Thr302ProfsTer?
ENST00000269703.7:c.904del	ENSP00000269703.1:p.Thr302ProfsTer?
ENST00000601005.2:c.904del	ENSP00000469866.1:p.Thr302ProfsTer?
NM_173483.3:c.904del	NP_775754.2:p.Thr302ProfsTer?
XM_011527692.1:c.904del	XP_011525994.1:p.Thr302ProfsTer?
XM_011527693.1:c.904del	XP_011525995.1:p.Thr302ProfsTer?
XM_011527692.2:c.904del	XP_011525994.1:p.Thr302ProfsTer?
XM_011527693.2:c.904del	XP_011525995.1:p.Thr302ProfsTer?
NM_173483.4:c.904del MANE Select	NP_775754.2:p.Thr302ProfsTer?