Canonical Allele Identifier: CA2406579480
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1931448008

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128807_42128809del , CM000684.2:g.42128807_42128809del GRCh38
NC_000022.10:g.42524809_42524811del , CM000684.1:g.42524809_42524811del GRCh37
NC_000022.9:g.40854753_40854755del NCBI36
NG_008376.3:g.6188_6190del
NG_008376.4:g.7007_7009del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360124.10:c.493_495del ENSP00000353241.6:p.Glu165del
ENST00000645361.2:c.646_648del MANE Select ENSP00000496150.1:p.Glu216del
ENST00000359033.4:c.493_495del ENSP00000351927.4:p.Glu165del
ENST00000360124.9:c.313_315del ENSP00000353241.5:p.Glu105del
ENST00000360608.9:c.646_648del ENSP00000353820.5:p.Glu216del
ENST00000389970.7:c.580_582del ENSP00000374620.4:p.Glu194del
ENST00000488442.1:n.1370_1372del
NM_000106.5:c.646_648del NP_000097.3:p.Glu216del
NM_001025161.2:c.493_495del NP_001020332.2:p.Glu165del
XM_011529966.1:c.646_648del XP_011528268.1:p.Glu216del
XM_011529967.1:c.646_648del XP_011528269.1:p.Glu216del
XM_011529968.1:c.646_648del XP_011528270.1:p.Glu216del
XM_011529969.1:c.502_504del XP_011528271.1:p.Glu168del
XM_011529970.1:c.493_495del XP_011528272.1:p.Glu165del
XM_011529971.1:c.502_504del XP_011528273.1:p.Glu168del
XM_011529972.1:c.646_648del XP_011528274.1:p.Glu216del
NM_000106.6:c.646_648del MANE Select NP_000097.3:p.Glu216del
NM_001025161.3:c.493_495del NP_001020332.2:p.Glu165del