Canonical Allele Identifier: CA2406578732
Gene: CYP2D6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42127854_42127855delinsGA , CM000684.2:g.42127854_42127855delinsGA GRCh38
NC_000022.10:g.42523856_42523857delinsGA , CM000684.1:g.42523856_42523857delinsGA GRCh37
NC_000022.9:g.40853800_40853801delinsGA NCBI36
NG_008376.3:g.7137_7138delinsTC
NG_008376.4:g.7956_7957delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.770_771delinsTC ENSP00000353241.6:n.770_771delinsTC
ENST00000645361.2:c.972_973delinsTC MANE Select ENSP00000496150.1:p.His324=
ENST00000359033.4:c.819_820delinsTC ENSP00000351927.4:p.His273=
ENST00000360124.9:c.590_591delinsTC ENSP00000353241.5:n.590_591delinsTC
ENST00000360608.9:c.972_973delinsTC ENSP00000353820.5:p.His324=
ENST00000389970.7:c.906_907delinsTC ENSP00000374620.4:p.His302=
ENST00000488442.1:n.1696_1697delinsTC
NM_000106.5:c.972_973delinsTC NP_000097.3:p.His324=
NM_001025161.2:c.819_820delinsTC NP_001020332.2:p.His273=
XM_011529966.1:c.972_973delinsTC XP_011528268.1:p.His324=
XM_011529967.1:c.972_973delinsTC XP_011528269.1:p.His324=
XM_011529968.1:c.972_973delinsTC XP_011528270.1:p.His324=
XM_011529969.1:c.828_829delinsTC XP_011528271.1:p.His276=
XM_011529970.1:c.819_820delinsTC XP_011528272.1:p.His273=
XM_011529971.1:c.828_829delinsTC XP_011528273.1:p.His276=
XM_011529972.1:c.844-221_844-220delinsTC XP_011528274.1:n.844-221_844-220delinsTC
NM_000106.6:c.972_973delinsTC MANE Select NP_000097.3:p.His324=
NM_001025161.3:c.819_820delinsTC NP_001020332.2:p.His273=