Canonical Allele Identifier: CA1025922351

Gene: CYP2D6

Linked Data

• dbSNP Id: rs780663872
• gnomAD v3: 22-42128755-C-CAG
• gnomAD v4: 22-42128755-C-CAG

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128759_42128760dup , CM000684.2:g.42128759_42128760dup	GRCh38
NC_000022.10:g.42524761_42524762dup , CM000684.1:g.42524761_42524762dup	GRCh37
NC_000022.9:g.40854705_40854706dup	NCBI36
NG_008376.3:g.6235_6236dup
NG_008376.4:g.7054_7055dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.513+27_513+28dup	ENSP00000353241.6:n.513+27_513+28dup
ENST00000645361.2:c.666+27_666+28dup MANE Select	ENSP00000496150.1:n.666+27_666+28dup
ENST00000359033.4:c.513+27_513+28dup	ENSP00000351927.4:n.513+27_513+28dup
ENST00000360124.9:c.333+27_333+28dup	ENSP00000353241.5:n.333+27_333+28dup
ENST00000360608.9:c.666+27_666+28dup	ENSP00000353820.5:n.666+27_666+28dup
ENST00000389970.7:c.600+27_600+28dup	ENSP00000374620.4:n.600+27_600+28dup
ENST00000488442.1:n.1390+27_1390+28dup
NM_000106.5:c.666+27_666+28dup	NP_000097.3:n.666+27_666+28dup
NM_001025161.2:c.513+27_513+28dup	NP_001020332.2:n.513+27_513+28dup
XM_011529966.1:c.666+27_666+28dup	XP_011528268.1:n.666+27_666+28dup
XM_011529967.1:c.666+27_666+28dup	XP_011528269.1:n.666+27_666+28dup
XM_011529968.1:c.666+27_666+28dup	XP_011528270.1:n.666+27_666+28dup
XM_011529969.1:c.522+27_522+28dup	XP_011528271.1:n.522+27_522+28dup
XM_011529970.1:c.513+27_513+28dup	XP_011528272.1:n.513+27_513+28dup
XM_011529971.1:c.522+27_522+28dup	XP_011528273.1:n.522+27_522+28dup
XM_011529972.1:c.666+27_666+28dup	XP_011528274.1:n.666+27_666+28dup
NM_000106.6:c.666+27_666+28dup MANE Select	NP_000097.3:n.666+27_666+28dup
NM_001025161.3:c.513+27_513+28dup	NP_001020332.2:n.513+27_513+28dup