Canonical Allele Identifier: CA2838446339

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128713A>T , CM000684.2:g.42128713A>T	GRCh38
NC_000022.10:g.42524715A>T , CM000684.1:g.42524715A>T	GRCh37
NC_000022.9:g.40854659A>T	NCBI36
NG_008376.3:g.6279T>A
NG_008376.4:g.7098T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.513+71T>A	ENSP00000353241.6:n.513+71T>A
ENST00000645361.2:c.666+71T>A MANE Select	ENSP00000496150.1:n.666+71T>A
ENST00000359033.4:c.513+71T>A	ENSP00000351927.4:n.513+71T>A
ENST00000360124.9:c.333+71T>A	ENSP00000353241.5:n.333+71T>A
ENST00000360608.9:c.666+71T>A	ENSP00000353820.5:n.666+71T>A
ENST00000389970.7:c.600+71T>A	ENSP00000374620.4:n.600+71T>A
ENST00000488442.1:n.1390+71T>A
NM_000106.5:c.666+71T>A	NP_000097.3:n.666+71T>A
NM_001025161.2:c.513+71T>A	NP_001020332.2:n.513+71T>A
XM_011529966.1:c.666+71T>A	XP_011528268.1:n.666+71T>A
XM_011529967.1:c.666+71T>A	XP_011528269.1:n.666+71T>A
XM_011529968.1:c.666+71T>A	XP_011528270.1:n.666+71T>A
XM_011529969.1:c.522+71T>A	XP_011528271.1:n.522+71T>A
XM_011529970.1:c.513+71T>A	XP_011528272.1:n.513+71T>A
XM_011529971.1:c.522+71T>A	XP_011528273.1:n.522+71T>A
XM_011529972.1:c.666+71T>A	XP_011528274.1:n.666+71T>A
NM_000106.6:c.666+71T>A MANE Select	NP_000097.3:n.666+71T>A
NM_001025161.3:c.513+71T>A	NP_001020332.2:n.513+71T>A