Canonical Allele Identifier: CA9269741

Gene: CYP4F22

Linked Data

• dbSNP Id: rs778228053
• ExAC: 19:15651541 C / CCTGGAGGGTGGAG
• MyVariant Identifiers: chr19:g.15651541_15651542insCTGGAGGGTGGAG (hg19) ; chr19:g.15540730_15540731insCTGGAGGGTGGAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540731_15540732insTGGAGGGTGGAGC , CM000681.2:g.15540731_15540732insTGGAGGGTGGAGC	GRCh38
NC_000019.9:g.15651542_15651543insTGGAGGGTGGAGC , CM000681.1:g.15651542_15651543insTGGAGGGTGGAGC	GRCh37
NC_000019.8:g.15512542_15512543insTGGAGGGTGGAGC	NCBI36
NG_007987.1:g.37207_37208insTGGAGGGTGGAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.939+14_939+15insTGGAGGGTGGAGC MANE Select	ENSP00000269703.1:n.939+14_939+15insTGGAGGGTGGAGC
ENST00000269703.7:c.939+14_939+15insTGGAGGGTGGAGC	ENSP00000269703.1:n.939+14_939+15insTGGAGGGTGGAGC
ENST00000601005.2:c.939+14_939+15insTGGAGGGTGGAGC	ENSP00000469866.1:n.939+14_939+15insTGGAGGGTGGAGC
NM_173483.3:c.939+14_939+15insTGGAGGGTGGAGC	NP_775754.2:n.939+14_939+15insTGGAGGGTGGAGC
XM_011527692.1:c.939+14_939+15insTGGAGGGTGGAGC	XP_011525994.1:n.939+14_939+15insTGGAGGGTGGAGC
XM_011527693.1:c.939+14_939+15insTGGAGGGTGGAGC	XP_011525995.1:n.939+14_939+15insTGGAGGGTGGAGC
XM_011527692.2:c.939+14_939+15insTGGAGGGTGGAGC	XP_011525994.1:n.939+14_939+15insTGGAGGGTGGAGC
XM_011527693.2:c.939+14_939+15insTGGAGGGTGGAGC	XP_011525995.1:n.939+14_939+15insTGGAGGGTGGAGC
NM_173483.4:c.939+14_939+15insTGGAGGGTGGAGC MANE Select	NP_775754.2:n.939+14_939+15insTGGAGGGTGGAGC