Canonical Allele Identifier: CA324673719
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs35029149
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42129503_42129504delinsCG , CM000684.2:g.42129503_42129504delinsCG GRCh38
NC_000022.10:g.42525505_42525506delinsCG , CM000684.1:g.42525505_42525506delinsCG GRCh37
NC_000022.9:g.40855449_40855450delinsCG NCBI36
NG_008376.3:g.5488_5489delinsCG
NG_008376.4:g.6307_6308delinsCG

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.352+234_352+235delinsCG ENSP00000353241.6:n.352+234_352+235delinsCG
ENST00000645361.2:c.352+234_352+235delinsCG MANE Select ENSP00000496150.1:n.352+234_352+235delinsCG
ENST00000359033.4:c.352+234_352+235delinsCG ENSP00000351927.4:n.352+234_352+235delinsCG
ENST00000360124.9:c.172+234_172+235delinsCG ENSP00000353241.5:n.172+234_172+235delinsCG
ENST00000360608.9:c.352+234_352+235delinsCG ENSP00000353820.5:n.352+234_352+235delinsCG
ENST00000389970.7:c.286+234_286+235delinsCG ENSP00000374620.4:n.286+234_286+235delinsCG
ENST00000488442.1:n.1076+234_1076+235delinsCG
NM_000106.5:c.352+234_352+235delinsCG NP_000097.3:n.352+234_352+235delinsCG
NM_001025161.2:c.352+234_352+235delinsCG NP_001020332.2:n.352+234_352+235delinsCG
XM_011529966.1:c.352+234_352+235delinsCG XP_011528268.1:n.352+234_352+235delinsCG
XM_011529967.1:c.352+234_352+235delinsCG XP_011528269.1:n.352+234_352+235delinsCG
XM_011529968.1:c.352+234_352+235delinsCG XP_011528270.1:n.352+234_352+235delinsCG
XM_011529969.1:c.209+234_209+235delinsCG XP_011528271.1:n.209+234_209+235delinsCG
XM_011529970.1:c.352+234_352+235delinsCG XP_011528272.1:n.352+234_352+235delinsCG
XM_011529971.1:c.209+234_209+235delinsCG XP_011528273.1:n.209+234_209+235delinsCG
XM_011529972.1:c.352+234_352+235delinsCG XP_011528274.1:n.352+234_352+235delinsCG
NM_000106.6:c.352+234_352+235delinsCG MANE Select NP_000097.3:n.352+234_352+235delinsCG
NM_001025161.3:c.352+234_352+235delinsCG NP_001020332.2:n.352+234_352+235delinsCG
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