Canonical Allele Identifier: CA2657036629

Gene: CYP2D6

Linked Data

• gnomAD v4: 22-42129411-CGCGGGCCCCGCGCCACCCACACTGAGCTTACAGCACAGGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42129416_42129455del , CM000684.2:g.42129416_42129455del	GRCh38
NC_000022.10:g.42525418_42525457del , CM000684.1:g.42525418_42525457del	GRCh37
NC_000022.9:g.40855362_40855401del	NCBI36
NG_008376.3:g.5541_5580del
NG_008376.4:g.6360_6399del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.352+287_352+326del	ENSP00000353241.6:n.352+287_352+326del
ENST00000645361.2:c.353-266_353-227del MANE Select	ENSP00000496150.1:n.353-266_353-227del
ENST00000359033.4:c.352+287_352+326del	ENSP00000351927.4:n.352+287_352+326del
ENST00000360124.9:c.172+287_172+326del	ENSP00000353241.5:n.172+287_172+326del
ENST00000360608.9:c.353-266_353-227del	ENSP00000353820.5:n.353-266_353-227del
ENST00000389970.7:c.287-266_287-227del	ENSP00000374620.4:n.287-266_287-227del
ENST00000488442.1:n.1077-266_1077-227del
NM_000106.5:c.353-266_353-227del	NP_000097.3:n.353-266_353-227del
NM_001025161.2:c.352+287_352+326del	NP_001020332.2:n.352+287_352+326del
XM_011529966.1:c.353-266_353-227del	XP_011528268.1:n.353-266_353-227del
XM_011529967.1:c.353-266_353-227del	XP_011528269.1:n.353-266_353-227del
XM_011529968.1:c.353-266_353-227del	XP_011528270.1:n.353-266_353-227del
XM_011529969.1:c.210-266_210-227del	XP_011528271.1:n.210-266_210-227del
XM_011529970.1:c.352+287_352+326del	XP_011528272.1:n.352+287_352+326del
XM_011529971.1:c.210-266_210-227del	XP_011528273.1:n.210-266_210-227del
XM_011529972.1:c.353-266_353-227del	XP_011528274.1:n.353-266_353-227del
NM_000106.6:c.353-266_353-227del MANE Select	NP_000097.3:n.353-266_353-227del
NM_001025161.3:c.352+287_352+326del	NP_001020332.2:n.352+287_352+326del