Canonical Allele Identifier: CA632129566

Gene: CYP4F22

Linked Data

• gnomAD v2: 19-15651448-CGTCAGCAGGGGG-C
• gnomAD v4: 19-15540637-CGTCAGCAGGGGG-C
• MyVariant Identifiers: chr19:g.15651449_15651460del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540638_15540649del , CM000681.2:g.15540638_15540649del	GRCh38
NC_000019.9:g.15651449_15651460del , CM000681.1:g.15651449_15651460del	GRCh37
NC_000019.8:g.15512449_15512460del	NCBI36
NG_007987.1:g.37114_37125del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.860_871del MANE Select	ENSP00000269703.1:p.Arg287_Ala291delinsPro
ENST00000269703.7:c.860_871del	ENSP00000269703.1:p.Arg287_Ala291delinsPro
ENST00000601005.2:c.860_871del	ENSP00000469866.1:p.Arg287_Ala291delinsPro
NM_173483.3:c.860_871del	NP_775754.2:p.Arg287_Ala291delinsPro
XM_011527692.1:c.860_871del	XP_011525994.1:p.Arg287_Ala291delinsPro
XM_011527693.1:c.860_871del	XP_011525995.1:p.Arg287_Ala291delinsPro
XM_011527692.2:c.860_871del	XP_011525994.1:p.Arg287_Ala291delinsPro
XM_011527693.2:c.860_871del	XP_011525995.1:p.Arg287_Ala291delinsPro
NM_173483.4:c.860_871del MANE Select	NP_775754.2:p.Arg287_Ala291delinsPro