Canonical Allele Identifier: CA2657031357
Gene: CYP2D6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42127849_42127853del , CM000684.2:g.42127849_42127853del GRCh38
NC_000022.10:g.42523851_42523855del , CM000684.1:g.42523851_42523855del GRCh37
NC_000022.9:g.40853795_40853799del NCBI36
NG_008376.3:g.7139_7143del
NG_008376.4:g.7958_7962del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360124.10:c.772_776del ENSP00000353241.6:n.772_776del
ENST00000645361.2:c.974_978del MANE Select ENSP00000496150.1:p.Pro325ArgfsTer23
ENST00000359033.4:c.821_825del ENSP00000351927.4:p.Pro274ArgfsTer23
ENST00000360124.9:c.592_596del ENSP00000353241.5:n.592_596del
ENST00000360608.9:c.974_978del ENSP00000353820.5:p.Pro325ArgfsTer23
ENST00000389970.7:c.908_912del ENSP00000374620.4:p.Pro303ArgfsTer?
ENST00000488442.1:n.1698_1702del
NM_000106.5:c.974_978del NP_000097.3:p.Pro325ArgfsTer23
NM_001025161.2:c.821_825del NP_001020332.2:p.Pro274ArgfsTer23
XM_011529966.1:c.974_978del XP_011528268.1:p.Pro325ArgfsTer23
XM_011529967.1:c.974_978del XP_011528269.1:p.Pro325ArgfsTer23
XM_011529968.1:c.974_978del XP_011528270.1:p.Pro325ArgfsTer23
XM_011529969.1:c.830_834del XP_011528271.1:p.Pro277ArgfsTer23
XM_011529970.1:c.821_825del XP_011528272.1:p.Pro274ArgfsTer23
XM_011529971.1:c.830_834del XP_011528273.1:p.Pro277ArgfsTer23
XM_011529972.1:c.844-219_844-215del XP_011528274.1:n.844-219_844-215del
NM_000106.6:c.974_978del MANE Select NP_000097.3:p.Pro325ArgfsTer23
NM_001025161.3:c.821_825del NP_001020332.2:p.Pro274ArgfsTer23