Canonical Allele Identifier: CA2406579037

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128241_42128242delinsCT , CM000684.2:g.42128241_42128242delinsCT	GRCh38
NC_000022.10:g.42524243_42524244delinsCT , CM000684.1:g.42524243_42524244delinsCT	GRCh37
NC_000022.9:g.40854187_40854188delinsCT	NCBI36
NG_008376.3:g.6750_6751delinsAG
NG_008376.4:g.7569_7570delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.622_623delinsAG	ENSP00000353241.6:p.Arg208=
ENST00000645361.2:c.775_776delinsAG MANE Select	ENSP00000496150.1:p.Arg259=
ENST00000359033.4:c.622_623delinsAG	ENSP00000351927.4:p.Arg208=
ENST00000360124.9:c.442_443delinsAG	ENSP00000353241.5:p.Arg148=
ENST00000360608.9:c.775_776delinsAG	ENSP00000353820.5:p.Arg259=
ENST00000389970.7:c.709_710delinsAG	ENSP00000374620.4:p.Arg237=
ENST00000488442.1:n.1499_1500delinsAG
NM_000106.5:c.775_776delinsAG	NP_000097.3:p.Arg259=
NM_001025161.2:c.622_623delinsAG	NP_001020332.2:p.Arg208=
XM_011529966.1:c.775_776delinsAG	XP_011528268.1:p.Arg259=
XM_011529967.1:c.775_776delinsAG	XP_011528269.1:p.Arg259=
XM_011529968.1:c.775_776delinsAG	XP_011528270.1:p.Arg259=
XM_011529969.1:c.631_632delinsAG	XP_011528271.1:p.Arg211=
XM_011529970.1:c.622_623delinsAG	XP_011528272.1:p.Arg208=
XM_011529971.1:c.631_632delinsAG	XP_011528273.1:p.Arg211=
XM_011529972.1:c.775_776delinsAG	XP_011528274.1:p.Arg259=
NM_000106.6:c.775_776delinsAG MANE Select	NP_000097.3:p.Arg259=
NM_001025161.3:c.622_623delinsAG	NP_001020332.2:p.Arg208=