Canonical Allele Identifier: CA1025922551

Gene: CYP2D6

Linked Data

• gnomAD v3: 22-42128936-A-AGGGGCGAAAGGGGCGAAG
• gnomAD v4: 22-42128936-A-AGGGGCGAAAGGGGCGAAG

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128942_42128943insAAAGGGGCGAAGGGGGCG , CM000684.2:g.42128942_42128943insAAAGGGGCGAAGGGGGCG	GRCh38
NC_000022.10:g.42524944_42524945insAAAGGGGCGAAGGGGGCG , CM000684.1:g.42524944_42524945insAAAGGGGCGAAGGGGGCG	GRCh37
NC_000022.9:g.40854888_40854889insAAAGGGGCGAAGGGGGCG	NCBI36
NG_008376.3:g.6055_6056insCTTCGCCCCTTTCGCCCC
NG_008376.4:g.6874_6875insCTTCGCCCCTTTCGCCCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.360_361insCTTCGCCCCTTTCGCCCC	ENSP00000353241.6:p.Pro120_Phe121insLeuAr...
ENST00000645361.2:c.513_514insCTTCGCCCCTTTCGCCCC MANE Select	ENSP00000496150.1:p.Pro171_Phe172insLeuAr...
ENST00000359033.4:c.360_361insCTTCGCCCCTTTCGCCCC	ENSP00000351927.4:p.Pro120_Phe121insLeuAr...
ENST00000360124.9:c.180_181insCTTCGCCCCTTTCGCCCC	ENSP00000353241.5:p.Pro60_Phe61insLeuArgP...
ENST00000360608.9:c.513_514insCTTCGCCCCTTTCGCCCC	ENSP00000353820.5:p.Pro171_Phe172insLeuAr...
ENST00000389970.7:c.447_448insCTTCGCCCCTTTCGCCCC	ENSP00000374620.4:p.Pro149_Phe150insLeuAr...
ENST00000488442.1:n.1237_1238insCTTCGCCCCTTTCGCCCC
NM_000106.5:c.513_514insCTTCGCCCCTTTCGCCCC	NP_000097.3:p.Pro171_Phe172insLeuArgProPh...
NM_001025161.2:c.360_361insCTTCGCCCCTTTCGCCCC	NP_001020332.2:p.Pro120_Phe121insLeuArgPr...
XM_011529966.1:c.513_514insCTTCGCCCCTTTCGCCCC	XP_011528268.1:p.Pro171_Phe172insLeuArgPr...
XM_011529967.1:c.513_514insCTTCGCCCCTTTCGCCCC	XP_011528269.1:p.Pro171_Phe172insLeuArgPr...
XM_011529968.1:c.513_514insCTTCGCCCCTTTCGCCCC	XP_011528270.1:p.Pro171_Phe172insLeuArgPr...
XM_011529969.1:c.369_370insCTTCGCCCCTTTCGCCCC	XP_011528271.1:p.Pro123_Phe124insLeuArgPr...
XM_011529970.1:c.360_361insCTTCGCCCCTTTCGCCCC	XP_011528272.1:p.Pro120_Phe121insLeuArgPr...
XM_011529971.1:c.369_370insCTTCGCCCCTTTCGCCCC	XP_011528273.1:p.Pro123_Phe124insLeuArgPr...
XM_011529972.1:c.513_514insCTTCGCCCCTTTCGCCCC	XP_011528274.1:p.Pro171_Phe172insLeuArgPr...
NM_000106.6:c.513_514insCTTCGCCCCTTTCGCCCC MANE Select	NP_000097.3:p.Pro171_Phe172insLeuArgProPh...
NM_001025161.3:c.360_361insCTTCGCCCCTTTCGCCCC	NP_001020332.2:p.Pro120_Phe121insLeuArgPr...