Canonical Allele Identifier: CA2657031391

Gene: CYP2D6

Linked Data

• gnomAD v4: 22-42130565-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42130565_42130566insC , CM000684.2:g.42130565_42130566insC	GRCh38
NC_000022.10:g.42526567_42526568insC , CM000684.1:g.42526567_42526568insC	GRCh37
NC_000022.9:g.40856511_40856512insC	NCBI36
NG_008376.3:g.4426_4427insG
NG_008376.4:g.5245_5246insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.180+46_180+47insG	ENSP00000353241.6:n.180+46_180+47insG
ENST00000645361.2:c.180+46_180+47insG MANE Select	ENSP00000496150.1:n.180+46_180+47insG
ENST00000359033.4:c.180+46_180+47insG	ENSP00000351927.4:n.180+46_180+47insG
ENST00000360608.9:c.180+46_180+47insG	ENSP00000353820.5:n.180+46_180+47insG
ENST00000389970.7:c.114+46_114+47insG	ENSP00000374620.4:n.114+46_114+47insG
ENST00000488442.1:n.248_249insG
NM_000106.5:c.180+46_180+47insG	NP_000097.3:n.180+46_180+47insG
NM_001025161.2:c.180+46_180+47insG	NP_001020332.2:n.180+46_180+47insG
XM_011529966.1:c.180+46_180+47insG	XP_011528268.1:n.180+46_180+47insG
XM_011529967.1:c.180+46_180+47insG	XP_011528269.1:n.180+46_180+47insG
XM_011529968.1:c.180+46_180+47insG	XP_011528270.1:n.180+46_180+47insG
XM_011529969.1:c.38-657_38-656insG	XP_011528271.1:n.38-657_38-656insG
XM_011529970.1:c.180+46_180+47insG	XP_011528272.1:n.180+46_180+47insG
XM_011529971.1:c.38-657_38-656insG	XP_011528273.1:n.38-657_38-656insG
XM_011529972.1:c.180+46_180+47insG	XP_011528274.1:n.180+46_180+47insG
XR_430455.2:n.207-2_207-1insC
NM_000106.6:c.180+46_180+47insG MANE Select	NP_000097.3:n.180+46_180+47insG
XR_002958749.1:n.154-2_154-1insC
NM_001025161.3:c.180+46_180+47insG	NP_001020332.2:n.180+46_180+47insG