Canonical Allele Identifier: CA2695228336

Gene: CYP4F22

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15540506_15540507delinsTA , CM000681.2:g.15540506_15540507delinsTA	GRCh38
NC_000019.9:g.15651317_15651318delinsTA , CM000681.1:g.15651317_15651318delinsTA	GRCh37
NC_000019.8:g.15512317_15512318delinsTA	NCBI36
NG_007987.1:g.36982_36983delinsTA

Transcript Alleles

HGVS	Amino-acid Change
NM_173483.4:c.728_729delinsTA MANE Select	NP_775754.2:p.Arg243Leu
ENST00000269703.8:c.728_729delinsTA MANE Select	ENSP00000269703.1:p.Arg243Leu
NM_173483.3:c.728_729delinsTA	NP_775754.2:p.Arg243Leu
ENST00000269703.7:c.728_729delinsTA	ENSP00000269703.1:p.Arg243Leu
ENST00000601005.2:c.728_729delinsTA	ENSP00000469866.1:p.Arg243Leu
XM_011527692.1:c.728_729delinsTA	XP_011525994.1:p.Arg243Leu
XM_011527692.2:c.728_729delinsTA	XP_011525994.1:p.Arg243Leu
XM_011527693.1:c.728_729delinsTA	XP_011525995.1:p.Arg243Leu
XM_011527693.2:c.728_729delinsTA	XP_011525995.1:p.Arg243Leu