Canonical Allele Identifier: CA2324927426

Gene: CYP4F22

Linked Data

• dbSNP Id: rs1971447305

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540619del , CM000681.2:g.15540619del	GRCh38
NC_000019.9:g.15651430del , CM000681.1:g.15651430del	GRCh37
NC_000019.8:g.15512430del	NCBI36
NG_007987.1:g.37095del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.841del MANE Select	ENSP00000269703.1:p.Glu281AsnfsTer?
ENST00000269703.7:c.841del	ENSP00000269703.1:p.Glu281AsnfsTer?
ENST00000601005.2:c.841del	ENSP00000469866.1:p.Glu281AsnfsTer?
NM_173483.3:c.841del	NP_775754.2:p.Glu281AsnfsTer?
XM_011527692.1:c.841del	XP_011525994.1:p.Glu281AsnfsTer?
XM_011527693.1:c.841del	XP_011525995.1:p.Glu281AsnfsTer?
XM_011527692.2:c.841del	XP_011525994.1:p.Glu281AsnfsTer?
XM_011527693.2:c.841del	XP_011525995.1:p.Glu281AsnfsTer?
NM_173483.4:c.841del MANE Select	NP_775754.2:p.Glu281AsnfsTer?