Canonical Allele Identifier: CA2406579008

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128211_42128214delinsCGGG , CM000684.2:g.42128211_42128214delinsCGGG	GRCh38
NC_000022.10:g.42524213_42524216delinsCGGG , CM000684.1:g.42524213_42524216delinsCGGG	GRCh37
NC_000022.9:g.40854157_40854160delinsCGGG	NCBI36
NG_008376.3:g.6778_6781delinsCCCG
NG_008376.4:g.7597_7600delinsCCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.650_653delinsCCCG	ENSP00000353241.6:p.Pro217=
ENST00000645361.2:c.803_806delinsCCCG MANE Select	ENSP00000496150.1:p.Pro268=
ENST00000359033.4:c.650_653delinsCCCG	ENSP00000351927.4:p.Pro217=
ENST00000360124.9:c.470_473delinsCCCG	ENSP00000353241.5:p.Pro157=
ENST00000360608.9:c.803_806delinsCCCG	ENSP00000353820.5:p.Pro268=
ENST00000389970.7:c.737_740delinsCCCG	ENSP00000374620.4:p.Pro246=
ENST00000488442.1:n.1527_1530delinsCCCG
NM_000106.5:c.803_806delinsCCCG	NP_000097.3:p.Pro268=
NM_001025161.2:c.650_653delinsCCCG	NP_001020332.2:p.Pro217=
XM_011529966.1:c.803_806delinsCCCG	XP_011528268.1:p.Pro268=
XM_011529967.1:c.803_806delinsCCCG	XP_011528269.1:p.Pro268=
XM_011529968.1:c.803_806delinsCCCG	XP_011528270.1:p.Pro268=
XM_011529969.1:c.659_662delinsCCCG	XP_011528271.1:p.Pro220=
XM_011529970.1:c.650_653delinsCCCG	XP_011528272.1:p.Pro217=
XM_011529971.1:c.659_662delinsCCCG	XP_011528273.1:p.Pro220=
XM_011529972.1:c.803_806delinsCCCG	XP_011528274.1:p.Pro268=
NM_000106.6:c.803_806delinsCCCG MANE Select	NP_000097.3:p.Pro268=
NM_001025161.3:c.650_653delinsCCCG	NP_001020332.2:p.Pro217=