Canonical Allele Identifier: CA2406578801
Gene: CYP2D6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42127947_42127948delinsTC , CM000684.2:g.42127947_42127948delinsTC GRCh38
NC_000022.10:g.42523949_42523950delinsTC , CM000684.1:g.42523949_42523950delinsTC GRCh37
NC_000022.9:g.40853893_40853894delinsTC NCBI36
NG_008376.3:g.7044_7045delinsGA
NG_008376.4:g.7863_7864delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.691-14_691-13delinsGA ENSP00000353241.6:n.691-14_691-13delinsGA...
ENST00000645361.2:c.879_880delinsGA MANE Select ENSP00000496150.1:p.Glu293=
ENST00000359033.4:c.726_727delinsGA ENSP00000351927.4:p.Glu242=
ENST00000360124.9:c.511-14_511-13delinsGA ENSP00000353241.5:n.511-14_511-13delinsGA...
ENST00000360608.9:c.879_880delinsGA ENSP00000353820.5:p.Glu293=
ENST00000389970.7:c.813_814delinsGA ENSP00000374620.4:p.Glu271=
ENST00000488442.1:n.1603_1604delinsGA
NM_000106.5:c.879_880delinsGA NP_000097.3:p.Glu293=
NM_001025161.2:c.726_727delinsGA NP_001020332.2:p.Glu242=
XM_011529966.1:c.879_880delinsGA XP_011528268.1:p.Glu293=
XM_011529967.1:c.879_880delinsGA XP_011528269.1:p.Glu293=
XM_011529968.1:c.879_880delinsGA XP_011528270.1:p.Glu293=
XM_011529969.1:c.735_736delinsGA XP_011528271.1:p.Glu245=
XM_011529970.1:c.726_727delinsGA XP_011528272.1:p.Glu242=
XM_011529971.1:c.735_736delinsGA XP_011528273.1:p.Glu245=
XM_011529972.1:c.843+226_843+227delinsGA XP_011528274.1:n.843+226_843+227delinsGA
NM_000106.6:c.879_880delinsGA MANE Select NP_000097.3:p.Glu293=
NM_001025161.3:c.726_727delinsGA NP_001020332.2:p.Glu242=