Canonical Allele Identifier: CA2406579010

Gene: CYP2D6

Linked Data

• dbSNP Id: rs72549352
• gnomAD v4: 22-42128211-CGGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128216_42128218del , CM000684.2:g.42128216_42128218del	GRCh38
NC_000022.10:g.42524218_42524220del , CM000684.1:g.42524218_42524220del	GRCh37
NC_000022.9:g.40854162_40854164del	NCBI36
NG_008376.3:g.6778_6780del
NG_008376.4:g.7597_7599del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.650_652del	ENSP00000353241.6:p.Pro217del
ENST00000645361.2:c.803_805del MANE Select	ENSP00000496150.1:p.Pro268del
ENST00000359033.4:c.650_652del	ENSP00000351927.4:p.Pro217del
ENST00000360124.9:c.470_472del	ENSP00000353241.5:p.Pro157del
ENST00000360608.9:c.803_805del	ENSP00000353820.5:p.Pro268del
ENST00000389970.7:c.737_739del	ENSP00000374620.4:p.Pro246del
ENST00000488442.1:n.1527_1529del
NM_000106.5:c.803_805del	NP_000097.3:p.Pro268del
NM_001025161.2:c.650_652del	NP_001020332.2:p.Pro217del
XM_011529966.1:c.803_805del	XP_011528268.1:p.Pro268del
XM_011529967.1:c.803_805del	XP_011528269.1:p.Pro268del
XM_011529968.1:c.803_805del	XP_011528270.1:p.Pro268del
XM_011529969.1:c.659_661del	XP_011528271.1:p.Pro220del
XM_011529970.1:c.650_652del	XP_011528272.1:p.Pro217del
XM_011529971.1:c.659_661del	XP_011528273.1:p.Pro220del
XM_011529972.1:c.803_805del	XP_011528274.1:p.Pro268del
NM_000106.6:c.803_805del MANE Select	NP_000097.3:p.Pro268del
NM_001025161.3:c.650_652del	NP_001020332.2:p.Pro217del