Canonical Allele Identifier: CA2657037738

Gene: CYP2D6

Linked Data

• gnomAD v4: 22-42129684-T-TCATCACCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42129686_42129694dup , CM000684.2:g.42129686_42129694dup	GRCh38
NC_000022.10:g.42525688_42525696dup , CM000684.1:g.42525688_42525696dup	GRCh37
NC_000022.9:g.40855632_40855640dup	NCBI36
NG_008376.3:g.5299_5307dup
NG_008376.4:g.6118_6126dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.352+45_352+53dup	ENSP00000353241.6:n.352+45_352+53dup
ENST00000645361.2:c.352+45_352+53dup MANE Select	ENSP00000496150.1:n.352+45_352+53dup
ENST00000359033.4:c.352+45_352+53dup	ENSP00000351927.4:n.352+45_352+53dup
ENST00000360124.9:c.172+45_172+53dup	ENSP00000353241.5:n.172+45_172+53dup
ENST00000360608.9:c.352+45_352+53dup	ENSP00000353820.5:n.352+45_352+53dup
ENST00000389970.7:c.286+45_286+53dup	ENSP00000374620.4:n.286+45_286+53dup
ENST00000488442.1:n.1076+45_1076+53dup
NM_000106.5:c.352+45_352+53dup	NP_000097.3:n.352+45_352+53dup
NM_001025161.2:c.352+45_352+53dup	NP_001020332.2:n.352+45_352+53dup
XM_011529966.1:c.352+45_352+53dup	XP_011528268.1:n.352+45_352+53dup
XM_011529967.1:c.352+45_352+53dup	XP_011528269.1:n.352+45_352+53dup
XM_011529968.1:c.352+45_352+53dup	XP_011528270.1:n.352+45_352+53dup
XM_011529969.1:c.209+45_209+53dup	XP_011528271.1:n.209+45_209+53dup
XM_011529970.1:c.352+45_352+53dup	XP_011528272.1:n.352+45_352+53dup
XM_011529971.1:c.209+45_209+53dup	XP_011528273.1:n.209+45_209+53dup
XM_011529972.1:c.352+45_352+53dup	XP_011528274.1:n.352+45_352+53dup
NM_000106.6:c.352+45_352+53dup MANE Select	NP_000097.3:n.352+45_352+53dup
NM_001025161.3:c.352+45_352+53dup	NP_001020332.2:n.352+45_352+53dup