Canonical Allele Identifier: CA2819054058
Gene: CYP2D6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128800del , CM000684.2:g.42128800del GRCh38
NC_000022.10:g.42524802del , CM000684.1:g.42524802del GRCh37
NC_000022.9:g.40854746del NCBI36
NG_008376.3:g.6192del
NG_008376.4:g.7011del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360124.10:c.497del ENSP00000353241.6:p.Ser166TrpfsTer8
ENST00000645361.2:c.650del MANE Select ENSP00000496150.1:p.Ser217TrpfsTer8
ENST00000359033.4:c.497del ENSP00000351927.4:p.Ser166TrpfsTer8
ENST00000360124.9:c.317del ENSP00000353241.5:p.Ser106TrpfsTer8
ENST00000360608.9:c.650del ENSP00000353820.5:p.Ser217TrpfsTer8
ENST00000389970.7:c.584del ENSP00000374620.4:p.Ser195TrpfsTer8
ENST00000488442.1:n.1374del
NM_000106.5:c.650del NP_000097.3:p.Ser217TrpfsTer8
NM_001025161.2:c.497del NP_001020332.2:p.Ser166TrpfsTer8
XM_011529966.1:c.650del XP_011528268.1:p.Ser217TrpfsTer8
XM_011529967.1:c.650del XP_011528269.1:p.Ser217TrpfsTer8
XM_011529968.1:c.650del XP_011528270.1:p.Ser217TrpfsTer8
XM_011529969.1:c.506del XP_011528271.1:p.Ser169TrpfsTer8
XM_011529970.1:c.497del XP_011528272.1:p.Ser166TrpfsTer8
XM_011529971.1:c.506del XP_011528273.1:p.Ser169TrpfsTer8
XM_011529972.1:c.650del XP_011528274.1:p.Ser217TrpfsTer8
NM_000106.6:c.650del MANE Select NP_000097.3:p.Ser217TrpfsTer8
NM_001025161.3:c.497del NP_001020332.2:p.Ser166TrpfsTer8