Canonical Allele Identifier: CA2738249612

Gene: CYP2D6

Linked Data

• dbSNP Id: rs2146932346

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127777del , CM000684.2:g.42127777del	GRCh38
NC_000022.10:g.42523779del , CM000684.1:g.42523779del	GRCh37
NC_000022.9:g.40853723del	NCBI36
NG_008376.3:g.7215del
NG_008376.4:g.8034del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.783+65del	ENSP00000353241.6:n.783+65del
ENST00000645361.2:c.985+65del MANE Select	ENSP00000496150.1:n.985+65del
ENST00000359033.4:c.832+65del	ENSP00000351927.4:n.832+65del
ENST00000360124.9:c.603+65del	ENSP00000353241.5:n.603+65del
ENST00000360608.9:c.985+65del	ENSP00000353820.5:n.985+65del
ENST00000389970.7:c.948+4del	ENSP00000374620.4:n.948+4del
ENST00000488442.1:n.1709+65del
NM_000106.5:c.985+65del	NP_000097.3:n.985+65del
NM_001025161.2:c.832+65del	NP_001020332.2:n.832+65del
XM_011529966.1:c.985+65del	XP_011528268.1:n.985+65del
XM_011529967.1:c.985+65del	XP_011528269.1:n.985+65del
XM_011529968.1:c.985+65del	XP_011528270.1:n.985+65del
XM_011529969.1:c.841+65del	XP_011528271.1:n.841+65del
XM_011529970.1:c.832+65del	XP_011528272.1:n.832+65del
XM_011529971.1:c.841+65del	XP_011528273.1:n.841+65del
XM_011529972.1:c.844-143del	XP_011528274.1:n.844-143del
NM_000106.6:c.985+65del MANE Select	NP_000097.3:n.985+65del
NM_001025161.3:c.832+65del	NP_001020332.2:n.832+65del