Canonical Allele Identifier: CA3244217401

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42129623C>G , CM000684.2:g.42129623C>G	GRCh38
NC_000022.10:g.42525625C>G , CM000684.1:g.42525625C>G	GRCh37
NC_000022.9:g.40855569C>G	NCBI36
NG_008376.3:g.5369G>C
NG_008376.4:g.6188G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000106.6:c.352+115G>C MANE Select	NP_000097.3:n.352+115G>C
ENST00000645361.2:c.352+115G>C MANE Select	ENSP00000496150.1:n.352+115G>C
NM_000106.5:c.352+115G>C	NP_000097.3:n.352+115G>C
NM_001025161.2:c.352+115G>C	NP_001020332.2:n.352+115G>C
NM_001025161.3:c.352+115G>C	NP_001020332.2:n.352+115G>C
ENST00000359033.4:c.352+115G>C	ENSP00000351927.4:n.352+115G>C
ENST00000360124.10:c.352+115G>C	ENSP00000353241.6:n.352+115G>C
ENST00000360124.9:c.172+115G>C	ENSP00000353241.5:n.172+115G>C
ENST00000360608.9:c.352+115G>C	ENSP00000353820.5:n.352+115G>C
ENST00000389970.7:c.286+115G>C	ENSP00000374620.4:n.286+115G>C
ENST00000488442.1:n.1076+115G>C
XM_011529966.1:c.352+115G>C	XP_011528268.1:n.352+115G>C
XM_011529967.1:c.352+115G>C	XP_011528269.1:n.352+115G>C
XM_011529968.1:c.352+115G>C	XP_011528270.1:n.352+115G>C
XM_011529969.1:c.209+115G>C	XP_011528271.1:n.209+115G>C
XM_011529970.1:c.352+115G>C	XP_011528272.1:n.352+115G>C
XM_011529971.1:c.209+115G>C	XP_011528273.1:n.209+115G>C
XM_011529972.1:c.352+115G>C	XP_011528274.1:n.352+115G>C