Canonical Allele Identifier: CA2987799607

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127846dup , CM000684.2:g.42127846dup	GRCh38
NC_000022.10:g.42523848dup , CM000684.1:g.42523848dup	GRCh37
NC_000022.9:g.40853792dup	NCBI36
NG_008376.3:g.7146dup
NG_008376.4:g.7965dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.779dup	ENSP00000353241.6:n.779dup
ENST00000645361.2:c.981dup MANE Select	ENSP00000496150.1:p.Gln328AlafsTer22
ENST00000359033.4:c.828dup	ENSP00000351927.4:p.Gln277AlafsTer22
ENST00000360124.9:c.599dup	ENSP00000353241.5:n.599dup
ENST00000360608.9:c.981dup	ENSP00000353820.5:p.Gln328AlafsTer22
ENST00000389970.7:c.915dup	ENSP00000374620.4:p.Gln306AlafsTer?
ENST00000488442.1:n.1705dup
NM_000106.5:c.981dup	NP_000097.3:p.Gln328AlafsTer22
NM_001025161.2:c.828dup	NP_001020332.2:p.Gln277AlafsTer22
XM_011529966.1:c.981dup	XP_011528268.1:p.Gln328AlafsTer22
XM_011529967.1:c.981dup	XP_011528269.1:p.Gln328AlafsTer22
XM_011529968.1:c.981dup	XP_011528270.1:p.Gln328AlafsTer22
XM_011529969.1:c.837dup	XP_011528271.1:p.Gln280AlafsTer22
XM_011529970.1:c.828dup	XP_011528272.1:p.Gln277AlafsTer22
XM_011529971.1:c.837dup	XP_011528273.1:p.Gln280AlafsTer22
XM_011529972.1:c.844-212dup	XP_011528274.1:n.844-212dup
NM_000106.6:c.981dup MANE Select	NP_000097.3:p.Gln328AlafsTer22
NM_001025161.3:c.828dup	NP_001020332.2:p.Gln277AlafsTer22