Canonical Allele Identifier: CA2406578769

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1749405014
• gnomAD v4: 22-42127905-CCAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127907_42127909del , CM000684.2:g.42127907_42127909del	GRCh38
NC_000022.10:g.42523909_42523911del , CM000684.1:g.42523909_42523911del	GRCh37
NC_000022.9:g.40853853_40853855del	NCBI36
NG_008376.3:g.7084_7086del
NG_008376.4:g.7903_7905del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.717_719del	ENSP00000353241.6:p.Trp240del
ENST00000645361.2:c.919_921del MANE Select	ENSP00000496150.1:p.Met307del
ENST00000359033.4:c.766_768del	ENSP00000351927.4:p.Met256del
ENST00000360124.9:c.537_539del	ENSP00000353241.5:p.Trp180del
ENST00000360608.9:c.919_921del	ENSP00000353820.5:p.Met307del
ENST00000389970.7:c.853_855del	ENSP00000374620.4:p.Met285del
ENST00000488442.1:n.1643_1645del
NM_000106.5:c.919_921del	NP_000097.3:p.Met307del
NM_001025161.2:c.766_768del	NP_001020332.2:p.Met256del
XM_011529966.1:c.919_921del	XP_011528268.1:p.Met307del
XM_011529967.1:c.919_921del	XP_011528269.1:p.Met307del
XM_011529968.1:c.919_921del	XP_011528270.1:p.Met307del
XM_011529969.1:c.775_777del	XP_011528271.1:p.Met259del
XM_011529970.1:c.766_768del	XP_011528272.1:p.Met256del
XM_011529971.1:c.775_777del	XP_011528273.1:p.Met259del
XM_011529972.1:c.843+266_843+268del	XP_011528274.1:n.843+266_843+268del
NM_000106.6:c.919_921del MANE Select	NP_000097.3:p.Met307del
NM_001025161.3:c.766_768del	NP_001020332.2:p.Met256del