Canonical Allele Identifier: CA2406578725
Gene: CYP2D6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42127845_42127864delinsGCACATCCGGATGTAGGATC , CM000684.2:g.42127845_42127864delinsGCACATCCGGATGTAGGATC GRCh38
NC_000022.10:g.42523847_42523866delinsGCACATCCGGATGTAGGATC , CM000684.1:g.42523847_42523866delinsGCACATCCGGATGTAGGATC GRCh37
NC_000022.9:g.40853791_40853810delinsGCACATCCGGATGTAGGATC NCBI36
NG_008376.3:g.7128_7147delinsGATCCTACATCCGGATGTGC
NG_008376.4:g.7947_7966delinsGATCCTACATCCGGATGTGC

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.761_780delinsGATCCTACATCCGGATGTGC ENSP00000353241.6:n.761_780delinsGATCCTAC...
ENST00000645361.2:c.963_982delinsGATCCTACATCCGGATGTGC MANE Select ENSP00000496150.1:p.Met321=
ENST00000359033.4:c.810_829delinsGATCCTACATCCGGATGTGC ENSP00000351927.4:p.Met270=
ENST00000360124.9:c.581_600delinsGATCCTACATCCGGATGTGC ENSP00000353241.5:n.581_600delinsGATCCTAC...
ENST00000360608.9:c.963_982delinsGATCCTACATCCGGATGTGC ENSP00000353820.5:p.Met321=
ENST00000389970.7:c.897_916delinsGATCCTACATCCGGATGTGC ENSP00000374620.4:p.Met299=
ENST00000488442.1:n.1687_1706delinsGATCCTACATCCGGATGTGC
NM_000106.5:c.963_982delinsGATCCTACATCCGGATGTGC NP_000097.3:p.Met321=
NM_001025161.2:c.810_829delinsGATCCTACATCCGGATGTGC NP_001020332.2:p.Met270=
XM_011529966.1:c.963_982delinsGATCCTACATCCGGATGTGC XP_011528268.1:p.Met321=
XM_011529967.1:c.963_982delinsGATCCTACATCCGGATGTGC XP_011528269.1:p.Met321=
XM_011529968.1:c.963_982delinsGATCCTACATCCGGATGTGC XP_011528270.1:p.Met321=
XM_011529969.1:c.819_838delinsGATCCTACATCCGGATGTGC XP_011528271.1:p.Met273=
XM_011529970.1:c.810_829delinsGATCCTACATCCGGATGTGC XP_011528272.1:p.Met270=
XM_011529971.1:c.819_838delinsGATCCTACATCCGGATGTGC XP_011528273.1:p.Met273=
XM_011529972.1:c.844-230_844-211delinsGATCCTACATCCGGATGTGC XP_011528274.1:n.844-230_844-211delinsGAT...
NM_000106.6:c.963_982delinsGATCCTACATCCGGATGTGC MANE Select NP_000097.3:p.Met321=
NM_001025161.3:c.810_829delinsGATCCTACATCCGGATGTGC NP_001020332.2:p.Met270=