Canonical Allele Identifier: CA2657033373
Gene: CYP2D6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128768_42128775del , CM000684.2:g.42128768_42128775del GRCh38
NC_000022.10:g.42524770_42524777del , CM000684.1:g.42524770_42524777del GRCh37
NC_000022.9:g.40854714_40854721del NCBI36
NG_008376.3:g.6221_6228del
NG_008376.4:g.7040_7047del

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.513+13_513+20del ENSP00000353241.6:n.513+13_513+20del
ENST00000645361.2:c.666+13_666+20del MANE Select ENSP00000496150.1:n.666+13_666+20del
ENST00000359033.4:c.513+13_513+20del ENSP00000351927.4:n.513+13_513+20del
ENST00000360124.9:c.333+13_333+20del ENSP00000353241.5:n.333+13_333+20del
ENST00000360608.9:c.666+13_666+20del ENSP00000353820.5:n.666+13_666+20del
ENST00000389970.7:c.600+13_600+20del ENSP00000374620.4:n.600+13_600+20del
ENST00000488442.1:n.1390+13_1390+20del
NM_000106.5:c.666+13_666+20del NP_000097.3:n.666+13_666+20del
NM_001025161.2:c.513+13_513+20del NP_001020332.2:n.513+13_513+20del
XM_011529966.1:c.666+13_666+20del XP_011528268.1:n.666+13_666+20del
XM_011529967.1:c.666+13_666+20del XP_011528269.1:n.666+13_666+20del
XM_011529968.1:c.666+13_666+20del XP_011528270.1:n.666+13_666+20del
XM_011529969.1:c.522+13_522+20del XP_011528271.1:n.522+13_522+20del
XM_011529970.1:c.513+13_513+20del XP_011528272.1:n.513+13_513+20del
XM_011529971.1:c.522+13_522+20del XP_011528273.1:n.522+13_522+20del
XM_011529972.1:c.666+13_666+20del XP_011528274.1:n.666+13_666+20del
NM_000106.6:c.666+13_666+20del MANE Select NP_000097.3:n.666+13_666+20del
NM_001025161.3:c.513+13_513+20del NP_001020332.2:n.513+13_513+20del