Canonical Allele Identifier: CA1025923840

Gene: CYP2D6

Linked Data

• gnomAD v3: 22-42130564-T-TG
• gnomAD v4: 22-42130564-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42130564_42130565insG , CM000684.2:g.42130564_42130565insG	GRCh38
NG_008376.3:g.4427_4428insC
NG_008376.4:g.5246_5247insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.180+47_180+48insC	ENSP00000353241.6:n.180+47_180+48insC
ENST00000645361.2:c.180+47_180+48insC MANE Select	ENSP00000496150.1:n.180+47_180+48insC
ENST00000359033.4:c.180+47_180+48insC	ENSP00000351927.4:n.180+47_180+48insC
ENST00000360608.9:c.180+47_180+48insC	ENSP00000353820.5:n.180+47_180+48insC
ENST00000389970.7:c.114+47_114+48insC	ENSP00000374620.4:n.114+47_114+48insC
ENST00000488442.1:n.249_250insC
NM_000106.5:c.180+47_180+48insC	NP_000097.3:n.180+47_180+48insC
NM_001025161.2:c.180+47_180+48insC	NP_001020332.2:n.180+47_180+48insC
XM_011529966.1:c.180+47_180+48insC	XP_011528268.1:n.180+47_180+48insC
XM_011529967.1:c.180+47_180+48insC	XP_011528269.1:n.180+47_180+48insC
XM_011529968.1:c.180+47_180+48insC	XP_011528270.1:n.180+47_180+48insC
XM_011529969.1:c.38-656_38-655insC	XP_011528271.1:n.38-656_38-655insC
XM_011529970.1:c.180+47_180+48insC	XP_011528272.1:n.180+47_180+48insC
XM_011529971.1:c.38-656_38-655insC	XP_011528273.1:n.38-656_38-655insC
XM_011529972.1:c.180+47_180+48insC	XP_011528274.1:n.180+47_180+48insC
XR_430455.2:n.207-3_207-2insG
NM_000106.6:c.180+47_180+48insC MANE Select	NP_000097.3:n.180+47_180+48insC
XR_002958749.1:n.154-3_154-2insG
NM_001025161.3:c.180+47_180+48insC	NP_001020332.2:n.180+47_180+48insC