Canonical Allele Identifier: CA2406579531
Gene: CYP2D6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128863T= , CM000684.2:g.42128863T= GRCh38
NC_000022.10:g.42524865T= , CM000684.1:g.42524865T= GRCh37
NC_000022.9:g.40854809T= NCBI36
NG_008376.3:g.6129A=
NG_008376.4:g.6948A=

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.434A= ENSP00000353241.6:p.Glu145=
ENST00000645361.2:c.587A= MANE Select ENSP00000496150.1:p.Glu196=
ENST00000359033.4:c.434A= ENSP00000351927.4:p.Glu145=
ENST00000360124.9:c.254A= ENSP00000353241.5:p.Glu85=
ENST00000360608.9:c.587A= ENSP00000353820.5:p.Glu196=
ENST00000389970.7:c.521A= ENSP00000374620.4:p.Glu174=
ENST00000488442.1:n.1311A=
NM_000106.5:c.587A= NP_000097.3:p.Glu196=
NM_001025161.2:c.434A= NP_001020332.2:p.Glu145=
XM_011529966.1:c.587A= XP_011528268.1:p.Glu196=
XM_011529967.1:c.587A= XP_011528269.1:p.Glu196=
XM_011529968.1:c.587A= XP_011528270.1:p.Glu196=
XM_011529969.1:c.443A= XP_011528271.1:p.Glu148=
XM_011529970.1:c.434A= XP_011528272.1:p.Glu145=
XM_011529971.1:c.443A= XP_011528273.1:p.Glu148=
XM_011529972.1:c.587A= XP_011528274.1:p.Glu196=
NM_000106.6:c.587A= MANE Select NP_000097.3:p.Glu196=
NM_001025161.3:c.434A= NP_001020332.2:p.Glu145=