Canonical Allele Identifier: CA2406578766
Gene: CYP2D6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42127902_42127905delinsTCAC , CM000684.2:g.42127902_42127905delinsTCAC GRCh38
NC_000022.10:g.42523904_42523907delinsTCAC , CM000684.1:g.42523904_42523907delinsTCAC GRCh37
NC_000022.9:g.40853848_40853851delinsTCAC NCBI36
NG_008376.3:g.7087_7090delinsGTGA
NG_008376.4:g.7906_7909delinsGTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000360124.10:c.720_723delinsGTGA ENSP00000353241.6:p.Trp240=
ENST00000645361.2:c.922_925delinsGTGA MANE Select ENSP00000496150.1:p.Val308=
ENST00000359033.4:c.769_772delinsGTGA ENSP00000351927.4:p.Val257=
ENST00000360124.9:c.540_543delinsGTGA ENSP00000353241.5:p.Trp180=
ENST00000360608.9:c.922_925delinsGTGA ENSP00000353820.5:p.Val308=
ENST00000389970.7:c.856_859delinsGTGA ENSP00000374620.4:p.Val286=
ENST00000488442.1:n.1646_1649delinsGTGA
NM_000106.5:c.922_925delinsGTGA NP_000097.3:p.Val308=
NM_001025161.2:c.769_772delinsGTGA NP_001020332.2:p.Val257=
XM_011529966.1:c.922_925delinsGTGA XP_011528268.1:p.Val308=
XM_011529967.1:c.922_925delinsGTGA XP_011528269.1:p.Val308=
XM_011529968.1:c.922_925delinsGTGA XP_011528270.1:p.Val308=
XM_011529969.1:c.778_781delinsGTGA XP_011528271.1:p.Val260=
XM_011529970.1:c.769_772delinsGTGA XP_011528272.1:p.Val257=
XM_011529971.1:c.778_781delinsGTGA XP_011528273.1:p.Val260=
XM_011529972.1:c.843+269_844-268delinsGTGA XP_011528274.1:n.843+269_844-268delinsGTGA
NM_000106.6:c.922_925delinsGTGA MANE Select NP_000097.3:p.Val308=
NM_001025161.3:c.769_772delinsGTGA NP_001020332.2:p.Val257=