Canonical Allele Identifier: CA2406579386
Gene: CYP2D6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128709_42128710delinsTC , CM000684.2:g.42128709_42128710delinsTC GRCh38
NC_000022.10:g.42524711_42524712delinsTC , CM000684.1:g.42524711_42524712delinsTC GRCh37
NC_000022.9:g.40854655_40854656delinsTC NCBI36
NG_008376.3:g.6282_6283delinsGA
NG_008376.4:g.7101_7102delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000360124.10:c.513+74_513+75delinsGA ENSP00000353241.6:n.513+74_513+75delinsGA
ENST00000645361.2:c.666+74_666+75delinsGA MANE Select ENSP00000496150.1:n.666+74_666+75delinsGA
ENST00000359033.4:c.513+74_513+75delinsGA ENSP00000351927.4:n.513+74_513+75delinsGA
ENST00000360124.9:c.333+74_333+75delinsGA ENSP00000353241.5:n.333+74_333+75delinsGA
ENST00000360608.9:c.666+74_666+75delinsGA ENSP00000353820.5:n.666+74_666+75delinsGA
ENST00000389970.7:c.600+74_600+75delinsGA ENSP00000374620.4:n.600+74_600+75delinsGA
ENST00000488442.1:n.1390+74_1390+75delinsGA
NM_000106.5:c.666+74_666+75delinsGA NP_000097.3:n.666+74_666+75delinsGA
NM_001025161.2:c.513+74_513+75delinsGA NP_001020332.2:n.513+74_513+75delinsGA
XM_011529966.1:c.666+74_666+75delinsGA XP_011528268.1:n.666+74_666+75delinsGA
XM_011529967.1:c.666+74_666+75delinsGA XP_011528269.1:n.666+74_666+75delinsGA
XM_011529968.1:c.666+74_666+75delinsGA XP_011528270.1:n.666+74_666+75delinsGA
XM_011529969.1:c.522+74_522+75delinsGA XP_011528271.1:n.522+74_522+75delinsGA
XM_011529970.1:c.513+74_513+75delinsGA XP_011528272.1:n.513+74_513+75delinsGA
XM_011529971.1:c.522+74_522+75delinsGA XP_011528273.1:n.522+74_522+75delinsGA
XM_011529972.1:c.666+74_666+75delinsGA XP_011528274.1:n.666+74_666+75delinsGA
NM_000106.6:c.666+74_666+75delinsGA MANE Select NP_000097.3:n.666+74_666+75delinsGA
NM_001025161.3:c.513+74_513+75delinsGA NP_001020332.2:n.513+74_513+75delinsGA