Canonical Allele Identifier: CA2657033654

Gene: CYP2D6

Linked Data

• gnomAD v4: 22-42128852-GGTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128858_42128860del , CM000684.2:g.42128858_42128860del	GRCh38
NC_000022.10:g.42524860_42524862del , CM000684.1:g.42524860_42524862del	GRCh37
NC_000022.9:g.40854804_40854806del	NCBI36
NG_008376.3:g.6137_6139del
NG_008376.4:g.6956_6958del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.442_444del	ENSP00000353241.6:p.Asp148del
ENST00000645361.2:c.595_597del MANE Select	ENSP00000496150.1:p.Asp199del
ENST00000359033.4:c.442_444del	ENSP00000351927.4:p.Asp148del
ENST00000360124.9:c.262_264del	ENSP00000353241.5:p.Asp88del
ENST00000360608.9:c.595_597del	ENSP00000353820.5:p.Asp199del
ENST00000389970.7:c.529_531del	ENSP00000374620.4:p.Asp177del
ENST00000488442.1:n.1319_1321del
NM_000106.5:c.595_597del	NP_000097.3:p.Asp199del
NM_001025161.2:c.442_444del	NP_001020332.2:p.Asp148del
XM_011529966.1:c.595_597del	XP_011528268.1:p.Asp199del
XM_011529967.1:c.595_597del	XP_011528269.1:p.Asp199del
XM_011529968.1:c.595_597del	XP_011528270.1:p.Asp199del
XM_011529969.1:c.451_453del	XP_011528271.1:p.Asp151del
XM_011529970.1:c.442_444del	XP_011528272.1:p.Asp148del
XM_011529971.1:c.451_453del	XP_011528273.1:p.Asp151del
XM_011529972.1:c.595_597del	XP_011528274.1:p.Asp199del
NM_000106.6:c.595_597del MANE Select	NP_000097.3:p.Asp199del
NM_001025161.3:c.442_444del	NP_001020332.2:p.Asp148del