Canonical Allele Identifier: CA2406579050

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128256_42128257delinsAG , CM000684.2:g.42128256_42128257delinsAG	GRCh38
NC_000022.10:g.42524258_42524259delinsAG , CM000684.1:g.42524258_42524259delinsAG	GRCh37
NC_000022.9:g.40854202_40854203delinsAG	NCBI36
NG_008376.3:g.6735_6736delinsCT
NG_008376.4:g.7554_7555delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.607_608delinsCT	ENSP00000353241.6:p.Leu203=
ENST00000645361.2:c.760_761delinsCT MANE Select	ENSP00000496150.1:p.Leu254=
ENST00000359033.4:c.607_608delinsCT	ENSP00000351927.4:p.Leu203=
ENST00000360124.9:c.427_428delinsCT	ENSP00000353241.5:p.Leu143=
ENST00000360608.9:c.760_761delinsCT	ENSP00000353820.5:p.Leu254=
ENST00000389970.7:c.694_695delinsCT	ENSP00000374620.4:p.Leu232=
ENST00000488442.1:n.1484_1485delinsCT
NM_000106.5:c.760_761delinsCT	NP_000097.3:p.Leu254=
NM_001025161.2:c.607_608delinsCT	NP_001020332.2:p.Leu203=
XM_011529966.1:c.760_761delinsCT	XP_011528268.1:p.Leu254=
XM_011529967.1:c.760_761delinsCT	XP_011528269.1:p.Leu254=
XM_011529968.1:c.760_761delinsCT	XP_011528270.1:p.Leu254=
XM_011529969.1:c.616_617delinsCT	XP_011528271.1:p.Leu206=
XM_011529970.1:c.607_608delinsCT	XP_011528272.1:p.Leu203=
XM_011529971.1:c.616_617delinsCT	XP_011528273.1:p.Leu206=
XM_011529972.1:c.760_761delinsCT	XP_011528274.1:p.Leu254=
NM_000106.6:c.760_761delinsCT MANE Select	NP_000097.3:p.Leu254=
NM_001025161.3:c.607_608delinsCT	NP_001020332.2:p.Leu203=