Canonical Allele Identifier: CA2324927967

Gene: CYP4F22

Linked Data

• dbSNP Id: rs1971451853

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540746_15540747insGCC , CM000681.2:g.15540746_15540747insGCC	GRCh38
NC_000019.9:g.15651557_15651558insGCC , CM000681.1:g.15651557_15651558insGCC	GRCh37
NC_000019.8:g.15512557_15512558insGCC	NCBI36
NG_007987.1:g.37222_37223insGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+29_939+30insGCC MANE Select	ENSP00000269703.1:n.939+29_939+30insGCC
ENST00000269703.7:c.939+29_939+30insGCC	ENSP00000269703.1:n.939+29_939+30insGCC
ENST00000601005.2:c.939+29_939+30insGCC	ENSP00000469866.1:n.939+29_939+30insGCC
NM_173483.3:c.939+29_939+30insGCC	NP_775754.2:n.939+29_939+30insGCC
XM_011527692.1:c.939+29_939+30insGCC	XP_011525994.1:n.939+29_939+30insGCC
XM_011527693.1:c.939+29_939+30insGCC	XP_011525995.1:n.939+29_939+30insGCC
XM_011527692.2:c.939+29_939+30insGCC	XP_011525994.1:n.939+29_939+30insGCC
XM_011527693.2:c.939+29_939+30insGCC	XP_011525995.1:n.939+29_939+30insGCC
NM_173483.4:c.939+29_939+30insGCC MANE Select	NP_775754.2:n.939+29_939+30insGCC