Canonical Allele Identifier: CA10652299

Gene: CYP4F22

Linked Data

• ClinVar Variation Id: 328442
• ClinVar RCV Id: RCV000293637 ; RCV001723915
• dbSNP Id: rs886054264
• MyVariant Identifiers: chr19:g.15651543_15651568delinsTGGAGGGTGGAGCCCTGCCTGGGA (hg19) ; chr19:g.15540732_15540757delinsTGGAGGGTGGAGCCCTGCCTGGGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540732_15540757delinsTGGAGGGTGGAGCCCTGCCTGGGA , CM000681.2:g.15540732_15540757delinsTGGAGGGTGGAGCCCTGCCTGGGA	GRCh38
NC_000019.9:g.15651543_15651568delinsTGGAGGGTGGAGCCCTGCCTGGGA , CM000681.1:g.15651543_15651568delinsTGGAGGGTGGAGCCCTGCCTGGGA	GRCh37
NC_000019.8:g.15512543_15512568delinsTGGAGGGTGGAGCCCTGCCTGGGA	NCBI36
NG_007987.1:g.37208_37233delinsTGGAGGGTGGAGCCCTGCCTGGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+15_939+40delinsTGGAGGGTGGAGCCCTGCCTGGGA MANE Select	ENSP00000269703.1:n.939+15_939+40delinsTGGAGGGTGGAGCCCTGCCTGG...
ENST00000269703.7:c.939+15_939+40delinsTGGAGGGTGGAGCCCTGCCTGGGA	ENSP00000269703.1:n.939+15_939+40delinsTGGAGGGTGGAGCCCTGCCTGG...
ENST00000601005.2:c.939+15_939+40delinsTGGAGGGTGGAGCCCTGCCTGGGA	ENSP00000469866.1:n.939+15_939+40delinsTGGAGGGTGGAGCCCTGCCTGG...
NM_173483.3:c.939+15_939+40delinsTGGAGGGTGGAGCCCTGCCTGGGA	NP_775754.2:n.939+15_939+40delinsTGGAGGGTGGAGCCCTGCCTGGGA
XM_011527692.1:c.939+15_939+40delinsTGGAGGGTGGAGCCCTGCCTGGGA	XP_011525994.1:n.939+15_939+40delinsTGGAGGGTGGAGCCCTGCCTGGGA
XM_011527693.1:c.939+15_939+40delinsTGGAGGGTGGAGCCCTGCCTGGGA	XP_011525995.1:n.939+15_939+40delinsTGGAGGGTGGAGCCCTGCCTGGGA
XM_011527692.2:c.939+15_939+40delinsTGGAGGGTGGAGCCCTGCCTGGGA	XP_011525994.1:n.939+15_939+40delinsTGGAGGGTGGAGCCCTGCCTGGGA
XM_011527693.2:c.939+15_939+40delinsTGGAGGGTGGAGCCCTGCCTGGGA	XP_011525995.1:n.939+15_939+40delinsTGGAGGGTGGAGCCCTGCCTGGGA
NM_173483.4:c.939+15_939+40delinsTGGAGGGTGGAGCCCTGCCTGGGA MANE Select	NP_775754.2:n.939+15_939+40delinsTGGAGGGTGGAGCCCTGCCTGGGA