Canonical Allele Identifier: CA2657029132

Gene: CYP2D6

Linked Data

• gnomAD v4: 22-42126566-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126570del , CM000684.2:g.42126570del	GRCh38
NC_000022.10:g.42522572del , CM000684.1:g.42522572del	GRCh37
NC_000022.9:g.40852516del	NCBI36
NG_008376.3:g.8425del
NG_008376.4:g.9244del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.1299del	ENSP00000353241.6:n.1299del
ENST00000645361.2:c.*7del MANE Select	ENSP00000496150.1:n.*7del
ENST00000359033.4:c.*7del	ENSP00000351927.4:n.*7del
ENST00000360124.9:c.1119del	ENSP00000353241.5:n.1119del
ENST00000360608.9:c.*7del	ENSP00000353820.5:n.*7del
ENST00000389970.7:c.*7del	ENSP00000374620.4:n.*7del
ENST00000488442.1:n.2225del
NM_000106.5:c.*7del	NP_000097.3:n.*7del
NM_001025161.2:c.*7del	NP_001020332.2:n.*7del
XM_011529966.1:c.1452+49del	XP_011528268.1:n.1452+49del
XM_011529967.1:c.1452+49del	XP_011528269.1:n.1452+49del
XM_011529968.1:c.1452+49del	XP_011528270.1:n.1452+49del
XM_011529969.1:c.1308+49del	XP_011528271.1:n.1308+49del
XM_011529970.1:c.1299+49del	XP_011528272.1:n.1299+49del
XM_011529971.1:c.*7del	XP_011528273.1:n.*7del
NM_000106.6:c.*7del MANE Select	NP_000097.3:n.*7del
NM_001025161.3:c.*7del	NP_001020332.2:n.*7del