Canonical Allele Identifier: CA2406579546
Gene: CYP2D6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128882_42128886delinsTGAGG , CM000684.2:g.42128882_42128886delinsTGAGG GRCh38
NC_000022.10:g.42524884_42524888delinsTGAGG , CM000684.1:g.42524884_42524888delinsTGAGG GRCh37
NC_000022.9:g.40854828_40854832delinsTGAGG NCBI36
NG_008376.3:g.6106_6110delinsCCTCA
NG_008376.4:g.6925_6929delinsCCTCA

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.411_415delinsCCTCA ENSP00000353241.6:p.Ser137=
ENST00000645361.2:c.564_568delinsCCTCA MANE Select ENSP00000496150.1:p.Ser188=
ENST00000359033.4:c.411_415delinsCCTCA ENSP00000351927.4:p.Ser137=
ENST00000360124.9:c.231_235delinsCCTCA ENSP00000353241.5:p.Ser77=
ENST00000360608.9:c.564_568delinsCCTCA ENSP00000353820.5:p.Ser188=
ENST00000389970.7:c.498_502delinsCCTCA ENSP00000374620.4:p.Ser166=
ENST00000488442.1:n.1288_1292delinsCCTCA
NM_000106.5:c.564_568delinsCCTCA NP_000097.3:p.Ser188=
NM_001025161.2:c.411_415delinsCCTCA NP_001020332.2:p.Ser137=
XM_011529966.1:c.564_568delinsCCTCA XP_011528268.1:p.Ser188=
XM_011529967.1:c.564_568delinsCCTCA XP_011528269.1:p.Ser188=
XM_011529968.1:c.564_568delinsCCTCA XP_011528270.1:p.Ser188=
XM_011529969.1:c.420_424delinsCCTCA XP_011528271.1:p.Ser140=
XM_011529970.1:c.411_415delinsCCTCA XP_011528272.1:p.Ser137=
XM_011529971.1:c.420_424delinsCCTCA XP_011528273.1:p.Ser140=
XM_011529972.1:c.564_568delinsCCTCA XP_011528274.1:p.Ser188=
NM_000106.6:c.564_568delinsCCTCA MANE Select NP_000097.3:p.Ser188=
NM_001025161.3:c.411_415delinsCCTCA NP_001020332.2:p.Ser137=