Canonical Allele Identifier: CA2324927950

Gene: CYP4F22

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540740_15540755delinsTGCTGGCCTCCCGAGG , CM000681.2:g.15540740_15540755delinsTGCTGGCCTCCCGAGG	GRCh38
NC_000019.9:g.15651551_15651566delinsTGCTGGCCTCCCGAGG , CM000681.1:g.15651551_15651566delinsTGCTGGCCTCCCGAGG	GRCh37
NC_000019.8:g.15512551_15512566delinsTGCTGGCCTCCCGAGG	NCBI36
NG_007987.1:g.37216_37231delinsTGCTGGCCTCCCGAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+23_939+38delinsTGCTGGCCTCCCGAGG MANE Select	ENSP00000269703.1:n.939+23_939+38delinsTGCTGGCCTCCCGAGG
ENST00000269703.7:c.939+23_939+38delinsTGCTGGCCTCCCGAGG	ENSP00000269703.1:n.939+23_939+38delinsTGCTGGCCTCCCGAGG
ENST00000601005.2:c.939+23_939+38delinsTGCTGGCCTCCCGAGG	ENSP00000469866.1:n.939+23_939+38delinsTGCTGGCCTCCCGAGG
NM_173483.3:c.939+23_939+38delinsTGCTGGCCTCCCGAGG	NP_775754.2:n.939+23_939+38delinsTGCTGGCCTCCCGAGG
XM_011527692.1:c.939+23_939+38delinsTGCTGGCCTCCCGAGG	XP_011525994.1:n.939+23_939+38delinsTGCTGGCCTCCCGAGG
XM_011527693.1:c.939+23_939+38delinsTGCTGGCCTCCCGAGG	XP_011525995.1:n.939+23_939+38delinsTGCTGGCCTCCCGAGG
XM_011527692.2:c.939+23_939+38delinsTGCTGGCCTCCCGAGG	XP_011525994.1:n.939+23_939+38delinsTGCTGGCCTCCCGAGG
XM_011527693.2:c.939+23_939+38delinsTGCTGGCCTCCCGAGG	XP_011525995.1:n.939+23_939+38delinsTGCTGGCCTCCCGAGG
NM_173483.4:c.939+23_939+38delinsTGCTGGCCTCCCGAGG MANE Select	NP_775754.2:n.939+23_939+38delinsTGCTGGCCTCCCGAGG