Canonical Allele Identifier: CA2406578681

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1931175409
• gnomAD v4: 22-42127785-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127790dup , CM000684.2:g.42127790dup	GRCh38
NC_000022.10:g.42523792dup , CM000684.1:g.42523792dup	GRCh37
NC_000022.9:g.40853736dup	NCBI36
NG_008376.3:g.7206dup
NG_008376.4:g.8025dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.783+56dup	ENSP00000353241.6:n.783+56dup
ENST00000645361.2:c.985+56dup MANE Select	ENSP00000496150.1:n.985+56dup
ENST00000359033.4:c.832+56dup	ENSP00000351927.4:n.832+56dup
ENST00000360124.9:c.603+56dup	ENSP00000353241.5:n.603+56dup
ENST00000360608.9:c.985+56dup	ENSP00000353820.5:n.985+56dup
ENST00000389970.7:c.943dup	ENSP00000374620.4:p.Ala315GlyfsTer?
ENST00000488442.1:n.1709+56dup
NM_000106.5:c.985+56dup	NP_000097.3:n.985+56dup
NM_001025161.2:c.832+56dup	NP_001020332.2:n.832+56dup
XM_011529966.1:c.985+56dup	XP_011528268.1:n.985+56dup
XM_011529967.1:c.985+56dup	XP_011528269.1:n.985+56dup
XM_011529968.1:c.985+56dup	XP_011528270.1:n.985+56dup
XM_011529969.1:c.841+56dup	XP_011528271.1:n.841+56dup
XM_011529970.1:c.832+56dup	XP_011528272.1:n.832+56dup
XM_011529971.1:c.841+56dup	XP_011528273.1:n.841+56dup
XM_011529972.1:c.844-152dup	XP_011528274.1:n.844-152dup
NM_000106.6:c.985+56dup MANE Select	NP_000097.3:n.985+56dup
NM_001025161.3:c.832+56dup	NP_001020332.2:n.832+56dup