Canonical Allele Identifier: CA639828305

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1569025187
• gnomAD v2: 22-42524979-T-TA
• gnomAD v4: 22-42128977-T-TA
• MyVariant Identifiers: chr22:g.42524979_42524980insA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128977_42128978insA , CM000684.2:g.42128977_42128978insA	GRCh38
NC_000022.10:g.42524979_42524980insA , CM000684.1:g.42524979_42524980insA	GRCh37
NC_000022.9:g.40854923_40854924insA	NCBI36
NG_008376.3:g.6014_6015insT
NG_008376.4:g.6833_6834insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.353-34_353-33insT	ENSP00000353241.6:n.353-34_353-33insT
ENST00000645361.2:c.506-34_506-33insT MANE Select	ENSP00000496150.1:n.506-34_506-33insT
ENST00000359033.4:c.353-34_353-33insT	ENSP00000351927.4:n.353-34_353-33insT
ENST00000360124.9:c.173-34_173-33insT	ENSP00000353241.5:n.173-34_173-33insT
ENST00000360608.9:c.506-34_506-33insT	ENSP00000353820.5:n.506-34_506-33insT
ENST00000389970.7:c.440-34_440-33insT	ENSP00000374620.4:n.440-34_440-33insT
ENST00000488442.1:n.1230-34_1230-33insT
NM_000106.5:c.506-34_506-33insT	NP_000097.3:n.506-34_506-33insT
NM_001025161.2:c.353-34_353-33insT	NP_001020332.2:n.353-34_353-33insT
XM_011529966.1:c.506-34_506-33insT	XP_011528268.1:n.506-34_506-33insT
XM_011529967.1:c.506-34_506-33insT	XP_011528269.1:n.506-34_506-33insT
XM_011529968.1:c.506-34_506-33insT	XP_011528270.1:n.506-34_506-33insT
XM_011529969.1:c.363-35_363-34insT	XP_011528271.1:n.363-35_363-34insT
XM_011529970.1:c.353-34_353-33insT	XP_011528272.1:n.353-34_353-33insT
XM_011529971.1:c.363-35_363-34insT	XP_011528273.1:n.363-35_363-34insT
XM_011529972.1:c.506-34_506-33insT	XP_011528274.1:n.506-34_506-33insT
NM_000106.6:c.506-34_506-33insT MANE Select	NP_000097.3:n.506-34_506-33insT
NM_001025161.3:c.353-34_353-33insT	NP_001020332.2:n.353-34_353-33insT