Canonical Allele Identifier: CA2813739241

Gene: CYP4F22

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540586_15540587insCCGTGCA , CM000681.2:g.15540586_15540587insCCGTGCA	GRCh38
NC_000019.9:g.15651397_15651398insCCGTGCA , CM000681.1:g.15651397_15651398insCCGTGCA	GRCh37
NC_000019.8:g.15512397_15512398insCCGTGCA	NCBI36
NG_007987.1:g.37062_37063insCCGTGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.808_809insCCGTGCA MANE Select	ENSP00000269703.1:p.Met270ThrfsTer10
ENST00000269703.7:c.808_809insCCGTGCA	ENSP00000269703.1:p.Met270ThrfsTer10
ENST00000601005.2:c.808_809insCCGTGCA	ENSP00000469866.1:p.Met270ThrfsTer10
NM_173483.3:c.808_809insCCGTGCA	NP_775754.2:p.Met270ThrfsTer10
XM_011527692.1:c.808_809insCCGTGCA	XP_011525994.1:p.Met270ThrfsTer10
XM_011527693.1:c.808_809insCCGTGCA	XP_011525995.1:p.Met270ThrfsTer10
XM_011527692.2:c.808_809insCCGTGCA	XP_011525994.1:p.Met270ThrfsTer10
XM_011527693.2:c.808_809insCCGTGCA	XP_011525995.1:p.Met270ThrfsTer10
NM_173483.4:c.808_809insCCGTGCA MANE Select	NP_775754.2:p.Met270ThrfsTer10