Canonical Allele Identifier: CA2406579876

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42129265_42129282delinsCCCCTGGTCTCCCGCAGT , CM000684.2:g.42129265_42129282delinsCCCCTGGTCTCCCGCAGT	GRCh38
NC_000022.10:g.42525267_42525284delinsCCCCTGGTCTCCCGCAGT , CM000684.1:g.42525267_42525284delinsCCCCTGGTCTCCCGCAGT	GRCh37
NC_000022.9:g.40855211_40855228delinsCCCCTGGTCTCCCGCAGT	NCBI36
NG_008376.3:g.5710_5727delinsACTGCGGGAGACCAGGGG
NG_008376.4:g.6529_6546delinsACTGCGGGAGACCAGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.353-338_353-321delinsACTGCGGGAGACCAGGGG	ENSP00000353241.6:n.353-338_353-321delinsACTGCGGGAGACCAGGGG
ENST00000645361.2:c.353-97_353-80delinsACTGCGGGAGACCAGGGG MANE Select	ENSP00000496150.1:n.353-97_353-80delinsACTGCGGGAGACCAGGGG
ENST00000359033.4:c.353-338_353-321delinsACTGCGGGAGACCAGGGG	ENSP00000351927.4:n.353-338_353-321delinsACTGCGGGAGACCAGGGG
ENST00000360124.9:c.173-338_173-321delinsACTGCGGGAGACCAGGGG	ENSP00000353241.5:n.173-338_173-321delinsACTGCGGGAGACCAGGGG
ENST00000360608.9:c.353-97_353-80delinsACTGCGGGAGACCAGGGG	ENSP00000353820.5:n.353-97_353-80delinsACTGCGGGAGACCAGGGG
ENST00000389970.7:c.287-97_287-80delinsACTGCGGGAGACCAGGGG	ENSP00000374620.4:n.287-97_287-80delinsACTGCGGGAGACCAGGGG
ENST00000488442.1:n.1077-97_1077-80delinsACTGCGGGAGACCAGGGG
NM_000106.5:c.353-97_353-80delinsACTGCGGGAGACCAGGGG	NP_000097.3:n.353-97_353-80delinsACTGCGGGAGACCAGGGG
NM_001025161.2:c.353-338_353-321delinsACTGCGGGAGACCAGGGG	NP_001020332.2:n.353-338_353-321delinsACTGCGGGAGACCAGGGG
XM_011529966.1:c.353-97_353-80delinsACTGCGGGAGACCAGGGG	XP_011528268.1:n.353-97_353-80delinsACTGCGGGAGACCAGGGG
XM_011529967.1:c.353-97_353-80delinsACTGCGGGAGACCAGGGG	XP_011528269.1:n.353-97_353-80delinsACTGCGGGAGACCAGGGG
XM_011529968.1:c.353-97_353-80delinsACTGCGGGAGACCAGGGG	XP_011528270.1:n.353-97_353-80delinsACTGCGGGAGACCAGGGG
XM_011529969.1:c.210-97_210-80delinsACTGCGGGAGACCAGGGG	XP_011528271.1:n.210-97_210-80delinsACTGCGGGAGACCAGGGG
XM_011529970.1:c.353-338_353-321delinsACTGCGGGAGACCAGGGG	XP_011528272.1:n.353-338_353-321delinsACTGCGGGAGACCAGGGG
XM_011529971.1:c.210-97_210-80delinsACTGCGGGAGACCAGGGG	XP_011528273.1:n.210-97_210-80delinsACTGCGGGAGACCAGGGG
XM_011529972.1:c.353-97_353-80delinsACTGCGGGAGACCAGGGG	XP_011528274.1:n.353-97_353-80delinsACTGCGGGAGACCAGGGG
NM_000106.6:c.353-97_353-80delinsACTGCGGGAGACCAGGGG MANE Select	NP_000097.3:n.353-97_353-80delinsACTGCGGGAGACCAGGGG
NM_001025161.3:c.353-338_353-321delinsACTGCGGGAGACCAGGGG	NP_001020332.2:n.353-338_353-321delinsACTGCGGGAGACCAGGGG