Canonical Allele Identifier: CA2738249457

Gene: CYP2D6

Linked Data

• dbSNP Id: rs2146932265

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127761del , CM000684.2:g.42127761del	GRCh38
NC_000022.10:g.42523763del , CM000684.1:g.42523763del	GRCh37
NC_000022.9:g.40853707del	NCBI36
NG_008376.3:g.7234del
NG_008376.4:g.8053del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.783+84del	ENSP00000353241.6:n.783+84del
ENST00000645361.2:c.985+84del MANE Select	ENSP00000496150.1:n.985+84del
ENST00000359033.4:c.832+84del	ENSP00000351927.4:n.832+84del
ENST00000360124.9:c.603+84del	ENSP00000353241.5:n.603+84del
ENST00000360608.9:c.985+84del	ENSP00000353820.5:n.985+84del
ENST00000389970.7:c.948+23del	ENSP00000374620.4:n.948+23del
ENST00000488442.1:n.1709+84del
NM_000106.5:c.985+84del	NP_000097.3:n.985+84del
NM_001025161.2:c.832+84del	NP_001020332.2:n.832+84del
XM_011529966.1:c.985+84del	XP_011528268.1:n.985+84del
XM_011529967.1:c.985+84del	XP_011528269.1:n.985+84del
XM_011529968.1:c.985+84del	XP_011528270.1:n.985+84del
XM_011529969.1:c.841+84del	XP_011528271.1:n.841+84del
XM_011529970.1:c.832+84del	XP_011528272.1:n.832+84del
XM_011529971.1:c.841+84del	XP_011528273.1:n.841+84del
XM_011529972.1:c.844-124del	XP_011528274.1:n.844-124del
NM_000106.6:c.985+84del MANE Select	NP_000097.3:n.985+84del
NM_001025161.3:c.832+84del	NP_001020332.2:n.832+84del