Canonical Allele Identifier: CA2406580831
Gene: CYP2D6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42130783_42130784delinsTA , CM000684.2:g.42130783_42130784delinsTA GRCh38
NC_000022.10:g.42526785_42526786delinsTA , CM000684.1:g.42526785_42526786delinsTA GRCh37
NC_000022.9:g.40856729_40856730delinsTA NCBI36
NG_008376.3:g.4208_4209delinsTA
NG_008376.4:g.5027_5028delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000360124.10:c.8_9delinsTA ENSP00000353241.6:p.Leu3=
ENST00000645361.2:c.8_9delinsTA MANE Select ENSP00000496150.1:p.Leu3=
ENST00000359033.4:c.8_9delinsTA ENSP00000351927.4:p.Leu3=
ENST00000360608.9:c.8_9delinsTA ENSP00000353820.5:p.Leu3=
ENST00000389970.7:c.-59_-58delinsTA ENSP00000374620.4:n.-59_-58delinsTA
ENST00000488442.1:n.30_31delinsTA
NM_000106.5:c.8_9delinsTA NP_000097.3:p.Leu3=
NM_001025161.2:c.8_9delinsTA NP_001020332.2:p.Leu3=
XM_011529966.1:c.8_9delinsTA XP_011528268.1:p.Leu3=
XM_011529967.1:c.8_9delinsTA XP_011528269.1:p.Leu3=
XM_011529968.1:c.8_9delinsTA XP_011528270.1:p.Leu3=
XM_011529969.1:c.37+513_37+514delinsTA XP_011528271.1:n.37+513_37+514delinsTA
XM_011529970.1:c.8_9delinsTA XP_011528272.1:p.Leu3=
XM_011529971.1:c.37+513_37+514delinsTA XP_011528273.1:n.37+513_37+514delinsTA
XM_011529972.1:c.8_9delinsTA XP_011528274.1:p.Leu3=
XR_430455.2:n.328+95_328+96delinsTA
NM_000106.6:c.8_9delinsTA MANE Select NP_000097.3:p.Leu3=
XR_002958749.1:n.275+95_275+96delinsTA
NM_001025161.3:c.8_9delinsTA NP_001020332.2:p.Leu3=