Canonical Allele Identifier: CA411773809
Gene: CYP2D6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128812A>C , CM000684.2:g.42128812A>C GRCh38
NC_000022.10:g.42524814A>C , CM000684.1:g.42524814A>C GRCh37
NC_000022.9:g.40854758A>C NCBI36
NG_008376.3:g.6180T>G
NG_008376.4:g.6999T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360124.10:c.485T>G ENSP00000353241.6:p.Leu162Arg
ENST00000645361.2:c.638T>G MANE Select ENSP00000496150.1:p.Leu213Arg
ENST00000359033.4:c.485T>G ENSP00000351927.4:p.Leu162Arg
ENST00000360124.9:c.305T>G ENSP00000353241.5:p.Leu102Arg
ENST00000360608.9:c.638T>G ENSP00000353820.5:p.Leu213Arg
ENST00000389970.7:c.572T>G ENSP00000374620.4:p.Leu191Arg
ENST00000488442.1:n.1362T>G
NM_000106.5:c.638T>G NP_000097.3:p.Leu213Arg
NM_001025161.2:c.485T>G NP_001020332.2:p.Leu162Arg
XM_011529966.1:c.638T>G XP_011528268.1:p.Leu213Arg
XM_011529967.1:c.638T>G XP_011528269.1:p.Leu213Arg
XM_011529968.1:c.638T>G XP_011528270.1:p.Leu213Arg
XM_011529969.1:c.494T>G XP_011528271.1:p.Leu165Arg
XM_011529970.1:c.485T>G XP_011528272.1:p.Leu162Arg
XM_011529971.1:c.494T>G XP_011528273.1:p.Leu165Arg
XM_011529972.1:c.638T>G XP_011528274.1:p.Leu213Arg
NM_000106.6:c.638T>G MANE Select NP_000097.3:p.Leu213Arg
NM_001025161.3:c.485T>G NP_001020332.2:p.Leu162Arg