Canonical Allele Identifier: CA411772348

Gene: CYP2D6

Linked Data

• MyVariant Identifiers: chr22:g.42523847G>T (hg19) ; chr22:g.42127845G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127845G>T , CM000684.2:g.42127845G>T	GRCh38
NC_000022.10:g.42523847G>T , CM000684.1:g.42523847G>T	GRCh37
NC_000022.9:g.40853791G>T	NCBI36
NG_008376.3:g.7147C>A
NG_008376.4:g.7966C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.780C>A	ENSP00000353241.6:n.780C>A
ENST00000645361.2:c.982C>A MANE Select	ENSP00000496150.1:p.Gln328Lys
ENST00000359033.4:c.829C>A	ENSP00000351927.4:p.Gln277Lys
ENST00000360124.9:c.600C>A	ENSP00000353241.5:n.600C>A
ENST00000360608.9:c.982C>A	ENSP00000353820.5:p.Gln328Lys
ENST00000389970.7:c.916C>A	ENSP00000374620.4:p.Gln306Lys
ENST00000488442.1:n.1706C>A
NM_000106.5:c.982C>A	NP_000097.3:p.Gln328Lys
NM_001025161.2:c.829C>A	NP_001020332.2:p.Gln277Lys
XM_011529966.1:c.982C>A	XP_011528268.1:p.Gln328Lys
XM_011529967.1:c.982C>A	XP_011528269.1:p.Gln328Lys
XM_011529968.1:c.982C>A	XP_011528270.1:p.Gln328Lys
XM_011529969.1:c.838C>A	XP_011528271.1:p.Gln280Lys
XM_011529970.1:c.829C>A	XP_011528272.1:p.Gln277Lys
XM_011529971.1:c.838C>A	XP_011528273.1:p.Gln280Lys
XM_011529972.1:c.844-211C>A	XP_011528274.1:n.844-211C>A
NM_000106.6:c.982C>A MANE Select	NP_000097.3:p.Gln328Lys
NM_001025161.3:c.829C>A	NP_001020332.2:p.Gln277Lys