Canonical Allele Identifier: CA2324927414

Gene: CYP4F22

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540613_15540614delinsAT , CM000681.2:g.15540613_15540614delinsAT	GRCh38
NC_000019.9:g.15651424_15651425delinsAT , CM000681.1:g.15651424_15651425delinsAT	GRCh37
NC_000019.8:g.15512424_15512425delinsAT	NCBI36
NG_007987.1:g.37089_37090delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269703.8:c.835_836delinsAT MANE Select	ENSP00000269703.1:p.Ile279=
ENST00000269703.7:c.835_836delinsAT	ENSP00000269703.1:p.Ile279=
ENST00000601005.2:c.835_836delinsAT	ENSP00000469866.1:p.Ile279=
NM_173483.3:c.835_836delinsAT	NP_775754.2:p.Ile279=
XM_011527692.1:c.835_836delinsAT	XP_011525994.1:p.Ile279=
XM_011527693.1:c.835_836delinsAT	XP_011525995.1:p.Ile279=
XM_011527692.2:c.835_836delinsAT	XP_011525994.1:p.Ile279=
XM_011527693.2:c.835_836delinsAT	XP_011525995.1:p.Ile279=
NM_173483.4:c.835_836delinsAT MANE Select	NP_775754.2:p.Ile279=