Canonical Allele Identifier: CA2324927433

Gene: CYP4F22

Linked Data

• dbSNP Id: rs1971447398

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540628_15540630del , CM000681.2:g.15540628_15540630del	GRCh38
NC_000019.9:g.15651439_15651441del , CM000681.1:g.15651439_15651441del	GRCh37
NC_000019.8:g.15512439_15512441del	NCBI36
NG_007987.1:g.37104_37106del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.850_852del MANE Select	ENSP00000269703.1:p.Arg284del
ENST00000269703.7:c.850_852del	ENSP00000269703.1:p.Arg284del
ENST00000601005.2:c.850_852del	ENSP00000469866.1:p.Arg284del
NM_173483.3:c.850_852del	NP_775754.2:p.Arg284del
XM_011527692.1:c.850_852del	XP_011525994.1:p.Arg284del
XM_011527693.1:c.850_852del	XP_011525995.1:p.Arg284del
XM_011527692.2:c.850_852del	XP_011525994.1:p.Arg284del
XM_011527693.2:c.850_852del	XP_011525995.1:p.Arg284del
NM_173483.4:c.850_852del MANE Select	NP_775754.2:p.Arg284del