Canonical Allele Identifier: CA324670978

Gene: CYP2D6

Linked Data

• dbSNP Id: rs267608296
• MyVariant Identifiers: chr22:g.42524219_42524220insC (hg19) ; chr22:g.42128217_42128218insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128217_42128218insC , CM000684.2:g.42128217_42128218insC	GRCh38
NC_000022.10:g.42524219_42524220insC , CM000684.1:g.42524219_42524220insC	GRCh37
NC_000022.9:g.40854163_40854164insC	NCBI36
NG_008376.3:g.6774_6775insG
NG_008376.4:g.7593_7594insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.646_647insG	ENSP00000353241.6:p.Pro216ArgfsTer7
ENST00000645361.2:c.799_800insG MANE Select	ENSP00000496150.1:p.Pro267ArgfsTer7
ENST00000359033.4:c.646_647insG	ENSP00000351927.4:p.Pro216ArgfsTer7
ENST00000360124.9:c.466_467insG	ENSP00000353241.5:p.Pro156ArgfsTer7
ENST00000360608.9:c.799_800insG	ENSP00000353820.5:p.Pro267ArgfsTer7
ENST00000389970.7:c.733_734insG	ENSP00000374620.4:p.Pro245ArgfsTer7
ENST00000488442.1:n.1523_1524insG
NM_000106.5:c.799_800insG	NP_000097.3:p.Pro267ArgfsTer7
NM_001025161.2:c.646_647insG	NP_001020332.2:p.Pro216ArgfsTer7
XM_011529966.1:c.799_800insG	XP_011528268.1:p.Pro267ArgfsTer7
XM_011529967.1:c.799_800insG	XP_011528269.1:p.Pro267ArgfsTer7
XM_011529968.1:c.799_800insG	XP_011528270.1:p.Pro267ArgfsTer7
XM_011529969.1:c.655_656insG	XP_011528271.1:p.Pro219ArgfsTer7
XM_011529970.1:c.646_647insG	XP_011528272.1:p.Pro216ArgfsTer7
XM_011529971.1:c.655_656insG	XP_011528273.1:p.Pro219ArgfsTer7
XM_011529972.1:c.799_800insG	XP_011528274.1:p.Pro267ArgfsTer7
NM_000106.6:c.799_800insG MANE Select	NP_000097.3:p.Pro267ArgfsTer7
NM_001025161.3:c.646_647insG	NP_001020332.2:p.Pro216ArgfsTer7