Canonical Allele Identifier: CA10264791
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs758912794

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42127953_42127955dup , CM000684.2:g.42127953_42127955dup GRCh38
NC_000022.10:g.42523955_42523957dup , CM000684.1:g.42523955_42523957dup GRCh37
NC_000022.9:g.40853899_40853901dup NCBI36
NG_008376.3:g.7041_7043dup
NG_008376.4:g.7860_7862dup

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.691-17_691-15dup ENSP00000353241.6:n.691-17_691-15dup
ENST00000645361.2:c.876_878dup MANE Select ENSP00000496150.1:p.Asp292_Glu293insAsp
ENST00000359033.4:c.723_725dup ENSP00000351927.4:p.Asp241_Glu242insAsp
ENST00000360124.9:c.511-17_511-15dup ENSP00000353241.5:n.511-17_511-15dup
ENST00000360608.9:c.876_878dup ENSP00000353820.5:p.Asp292_Glu293insAsp
ENST00000389970.7:c.810_812dup ENSP00000374620.4:p.Asp270_Glu271insAsp
ENST00000488442.1:n.1600_1602dup
NM_000106.5:c.876_878dup NP_000097.3:p.Asp292_Glu293insAsp
NM_001025161.2:c.723_725dup NP_001020332.2:p.Asp241_Glu242insAsp
XM_011529966.1:c.876_878dup XP_011528268.1:p.Asp292_Glu293insAsp
XM_011529967.1:c.876_878dup XP_011528269.1:p.Asp292_Glu293insAsp
XM_011529968.1:c.876_878dup XP_011528270.1:p.Asp292_Glu293insAsp
XM_011529969.1:c.732_734dup XP_011528271.1:p.Asp244_Glu245insAsp
XM_011529970.1:c.723_725dup XP_011528272.1:p.Asp241_Glu242insAsp
XM_011529971.1:c.732_734dup XP_011528273.1:p.Asp244_Glu245insAsp
XM_011529972.1:c.843+223_843+225dup XP_011528274.1:n.843+223_843+225dup
NM_000106.6:c.876_878dup MANE Select NP_000097.3:p.Asp292_Glu293insAsp
NM_001025161.3:c.723_725dup NP_001020332.2:p.Asp241_Glu242insAsp