Canonical Allele Identifier: CA2406578917

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128105_42128117delinsGCCTCCCCTCATT , CM000684.2:g.42128105_42128117delinsGCCTCCCCTCATT	GRCh38
NC_000022.10:g.42524107_42524119delinsGCCTCCCCTCATT , CM000684.1:g.42524107_42524119delinsGCCTCCCCTCATT	GRCh37
NC_000022.9:g.40854051_40854063delinsGCCTCCCCTCATT	NCBI36
NG_008376.3:g.6875_6887delinsAATGAGGGGAGGC
NG_008376.4:g.7694_7706delinsAATGAGGGGAGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.690+57_690+69delinsAATGAGGGGAGGC	ENSP00000353241.6:n.690+57_690+69delinsAATGAGGGGAGGC
ENST00000645361.2:c.843+57_843+69delinsAATGAGGGGAGGC MANE Select	ENSP00000496150.1:n.843+57_843+69delinsAATGAGGGGAGGC
ENST00000359033.4:c.690+57_690+69delinsAATGAGGGGAGGC	ENSP00000351927.4:n.690+57_690+69delinsAATGAGGGGAGGC
ENST00000360124.9:c.510+57_510+69delinsAATGAGGGGAGGC	ENSP00000353241.5:n.510+57_510+69delinsAATGAGGGGAGGC
ENST00000360608.9:c.843+57_843+69delinsAATGAGGGGAGGC	ENSP00000353820.5:n.843+57_843+69delinsAATGAGGGGAGGC
ENST00000389970.7:c.777+57_777+69delinsAATGAGGGGAGGC	ENSP00000374620.4:n.777+57_777+69delinsAATGAGGGGAGGC
ENST00000488442.1:n.1567+57_1567+69delinsAATGAGGGGAGGC
NM_000106.5:c.843+57_843+69delinsAATGAGGGGAGGC	NP_000097.3:n.843+57_843+69delinsAATGAGGGGAGGC
NM_001025161.2:c.690+57_690+69delinsAATGAGGGGAGGC	NP_001020332.2:n.690+57_690+69delinsAATGAGGGGAGGC
XM_011529966.1:c.843+57_843+69delinsAATGAGGGGAGGC	XP_011528268.1:n.843+57_843+69delinsAATGAGGGGAGGC
XM_011529967.1:c.843+57_843+69delinsAATGAGGGGAGGC	XP_011528269.1:n.843+57_843+69delinsAATGAGGGGAGGC
XM_011529968.1:c.843+57_843+69delinsAATGAGGGGAGGC	XP_011528270.1:n.843+57_843+69delinsAATGAGGGGAGGC
XM_011529969.1:c.699+57_699+69delinsAATGAGGGGAGGC	XP_011528271.1:n.699+57_699+69delinsAATGAGGGGAGGC
XM_011529970.1:c.690+57_690+69delinsAATGAGGGGAGGC	XP_011528272.1:n.690+57_690+69delinsAATGAGGGGAGGC
XM_011529971.1:c.699+57_699+69delinsAATGAGGGGAGGC	XP_011528273.1:n.699+57_699+69delinsAATGAGGGGAGGC
XM_011529972.1:c.843+57_843+69delinsAATGAGGGGAGGC	XP_011528274.1:n.843+57_843+69delinsAATGAGGGGAGGC
NM_000106.6:c.843+57_843+69delinsAATGAGGGGAGGC MANE Select	NP_000097.3:n.843+57_843+69delinsAATGAGGGGAGGC
NM_001025161.3:c.690+57_690+69delinsAATGAGGGGAGGC	NP_001020332.2:n.690+57_690+69delinsAATGAGGGGAGGC