Canonical Allele Identifier: CA2406579103

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128332_42128334delinsCGG , CM000684.2:g.42128332_42128334delinsCGG	GRCh38
NC_000022.10:g.42524334_42524336delinsCGG , CM000684.1:g.42524334_42524336delinsCGG	GRCh37
NC_000022.9:g.40854278_40854280delinsCGG	NCBI36
NG_008376.3:g.6658_6660delinsCCG
NG_008376.4:g.7477_7479delinsCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.530_532delinsCCG	ENSP00000353241.6:p.Pro177=
ENST00000645361.2:c.683_685delinsCCG MANE Select	ENSP00000496150.1:p.Pro228=
ENST00000359033.4:c.530_532delinsCCG	ENSP00000351927.4:p.Pro177=
ENST00000360124.9:c.350_352delinsCCG	ENSP00000353241.5:p.Pro117=
ENST00000360608.9:c.683_685delinsCCG	ENSP00000353820.5:p.Pro228=
ENST00000389970.7:c.617_619delinsCCG	ENSP00000374620.4:p.Pro206=
ENST00000488442.1:n.1407_1409delinsCCG
NM_000106.5:c.683_685delinsCCG	NP_000097.3:p.Pro228=
NM_001025161.2:c.530_532delinsCCG	NP_001020332.2:p.Pro177=
XM_011529966.1:c.683_685delinsCCG	XP_011528268.1:p.Pro228=
XM_011529967.1:c.683_685delinsCCG	XP_011528269.1:p.Pro228=
XM_011529968.1:c.683_685delinsCCG	XP_011528270.1:p.Pro228=
XM_011529969.1:c.539_541delinsCCG	XP_011528271.1:p.Pro180=
XM_011529970.1:c.530_532delinsCCG	XP_011528272.1:p.Pro177=
XM_011529971.1:c.539_541delinsCCG	XP_011528273.1:p.Pro180=
XM_011529972.1:c.683_685delinsCCG	XP_011528274.1:p.Pro228=
NM_000106.6:c.683_685delinsCCG MANE Select	NP_000097.3:p.Pro228=
NM_001025161.3:c.530_532delinsCCG	NP_001020332.2:p.Pro177=