Canonical Allele Identifier: CA2406580770

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42130366_42130383delinsATGGGCTTGCATGCCCAC , CM000684.2:g.42130366_42130383delinsATGGGCTTGCATGCCCAC	GRCh38
NC_000022.10:g.42526368_42526385delinsATGGGCTTGCATGCCCAC , CM000684.1:g.42526368_42526385delinsATGGGCTTGCATGCCCAC	GRCh37
NC_000022.9:g.40856312_40856329delinsATGGGCTTGCATGCCCAC	NCBI36
NG_008376.3:g.4609_4626delinsGTGGGCATGCAAGCCCAT
NG_008376.4:g.5428_5445delinsGTGGGCATGCAAGCCCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.180+229_180+246delinsGTGGGCATGCAAGCCCAT	ENSP00000353241.6:n.180+229_180+246delinsGTGGGCATGCAAGCCCAT
ENST00000645361.2:c.180+229_180+246delinsGTGGGCATGCAAGCCCAT MANE Select	ENSP00000496150.1:n.180+229_180+246delinsGTGGGCATGCAAGCCCAT
ENST00000359033.4:c.180+229_180+246delinsGTGGGCATGCAAGCCCAT	ENSP00000351927.4:n.180+229_180+246delinsGTGGGCATGCAAGCCCAT
ENST00000360608.9:c.180+229_180+246delinsGTGGGCATGCAAGCCCAT	ENSP00000353820.5:n.180+229_180+246delinsGTGGGCATGCAAGCCCAT
ENST00000389970.7:c.114+229_114+246delinsGTGGGCATGCAAGCCCAT	ENSP00000374620.4:n.114+229_114+246delinsGTGGGCATGCAAGCCCAT
ENST00000488442.1:n.431_448delinsGTGGGCATGCAAGCCCAT
NM_000106.5:c.180+229_180+246delinsGTGGGCATGCAAGCCCAT	NP_000097.3:n.180+229_180+246delinsGTGGGCATGCAAGCCCAT
NM_001025161.2:c.180+229_180+246delinsGTGGGCATGCAAGCCCAT	NP_001020332.2:n.180+229_180+246delinsGTGGGCATGCAAGCCCAT
XM_011529966.1:c.180+229_180+246delinsGTGGGCATGCAAGCCCAT	XP_011528268.1:n.180+229_180+246delinsGTGGGCATGCAAGCCCAT
XM_011529967.1:c.180+229_180+246delinsGTGGGCATGCAAGCCCAT	XP_011528269.1:n.180+229_180+246delinsGTGGGCATGCAAGCCCAT
XM_011529968.1:c.180+229_180+246delinsGTGGGCATGCAAGCCCAT	XP_011528270.1:n.180+229_180+246delinsGTGGGCATGCAAGCCCAT
XM_011529969.1:c.38-474_38-457delinsGTGGGCATGCAAGCCCAT	XP_011528271.1:n.38-474_38-457delinsGTGGGCATGCAAGCCCAT
XM_011529970.1:c.180+229_180+246delinsGTGGGCATGCAAGCCCAT	XP_011528272.1:n.180+229_180+246delinsGTGGGCATGCAAGCCCAT
XM_011529971.1:c.38-474_38-457delinsGTGGGCATGCAAGCCCAT	XP_011528273.1:n.38-474_38-457delinsGTGGGCATGCAAGCCCAT
XM_011529972.1:c.180+229_180+246delinsGTGGGCATGCAAGCCCAT	XP_011528274.1:n.180+229_180+246delinsGTGGGCATGCAAGCCCAT
XR_430455.2:n.206+143_206+160delinsATGGGCTTGCATGCCCAC
NM_000106.6:c.180+229_180+246delinsGTGGGCATGCAAGCCCAT MANE Select	NP_000097.3:n.180+229_180+246delinsGTGGGCATGCAAGCCCAT
XR_002958749.1:n.153+143_153+160delinsATGGGCTTGCATGCCCAC
NM_001025161.3:c.180+229_180+246delinsGTGGGCATGCAAGCCCAT	NP_001020332.2:n.180+229_180+246delinsGTGGGCATGCAAGCCCAT