Canonical Allele Identifier: CA2406578605

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127675_42127686delinsGGGTCCGGCCCT , CM000684.2:g.42127675_42127686delinsGGGTCCGGCCCT	GRCh38
NC_000022.10:g.42523677_42523688delinsGGGTCCGGCCCT , CM000684.1:g.42523677_42523688delinsGGGTCCGGCCCT	GRCh37
NC_000022.9:g.40853621_40853632delinsGGGTCCGGCCCT	NCBI36
NG_008376.3:g.7306_7317delinsAGGGCCGGACCC
NG_008376.4:g.8125_8136delinsAGGGCCGGACCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.784-52_784-41delinsAGGGCCGGACCC	ENSP00000353241.6:n.784-52_784-41delinsAGGGCCGGACCC
ENST00000645361.2:c.986-52_986-41delinsAGGGCCGGACCC MANE Select	ENSP00000496150.1:n.986-52_986-41delinsAGGGCCGGACCC
ENST00000359033.4:c.833-52_833-41delinsAGGGCCGGACCC	ENSP00000351927.4:n.833-52_833-41delinsAGGGCCGGACCC
ENST00000360124.9:c.604-52_604-41delinsAGGGCCGGACCC	ENSP00000353241.5:n.604-52_604-41delinsAGGGCCGGACCC
ENST00000360608.9:c.986-52_986-41delinsAGGGCCGGACCC	ENSP00000353820.5:n.986-52_986-41delinsAGGGCCGGACCC
ENST00000389970.7:c.949-24_949-13delinsAGGGCCGGACCC	ENSP00000374620.4:n.949-24_949-13delinsAGGGCCGGACCC
ENST00000488442.1:n.1710-52_1710-41delinsAGGGCCGGACCC
NM_000106.5:c.986-52_986-41delinsAGGGCCGGACCC	NP_000097.3:n.986-52_986-41delinsAGGGCCGGACCC
NM_001025161.2:c.833-52_833-41delinsAGGGCCGGACCC	NP_001020332.2:n.833-52_833-41delinsAGGGCCGGACCC
XM_011529966.1:c.986-52_986-41delinsAGGGCCGGACCC	XP_011528268.1:n.986-52_986-41delinsAGGGCCGGACCC
XM_011529967.1:c.986-52_986-41delinsAGGGCCGGACCC	XP_011528269.1:n.986-52_986-41delinsAGGGCCGGACCC
XM_011529968.1:c.986-52_986-41delinsAGGGCCGGACCC	XP_011528270.1:n.986-52_986-41delinsAGGGCCGGACCC
XM_011529969.1:c.842-52_842-41delinsAGGGCCGGACCC	XP_011528271.1:n.842-52_842-41delinsAGGGCCGGACCC
XM_011529970.1:c.833-52_833-41delinsAGGGCCGGACCC	XP_011528272.1:n.833-52_833-41delinsAGGGCCGGACCC
XM_011529971.1:c.842-52_842-41delinsAGGGCCGGACCC	XP_011528273.1:n.842-52_842-41delinsAGGGCCGGACCC
XM_011529972.1:c.844-52_844-41delinsAGGGCCGGACCC	XP_011528274.1:n.844-52_844-41delinsAGGGCCGGACCC
NM_000106.6:c.986-52_986-41delinsAGGGCCGGACCC MANE Select	NP_000097.3:n.986-52_986-41delinsAGGGCCGGACCC
NM_001025161.3:c.833-52_833-41delinsAGGGCCGGACCC	NP_001020332.2:n.833-52_833-41delinsAGGGCCGGACCC