Canonical Allele Identifier: CA753329227

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1489656677
• MyVariant Identifiers: chr22:g.42127903_42127905del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127905_42127907del , CM000684.2:g.42127905_42127907del	GRCh38
NC_000022.10:g.42523907_42523909del , CM000684.1:g.42523907_42523909del	GRCh37
NC_000022.9:g.40853851_40853853del	NCBI36
NG_008376.3:g.7087_7089del
NG_008376.4:g.7906_7908del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.720_722del	ENSP00000353241.6:p.Trp240Ter
ENST00000645361.2:c.922_924del MANE Select	ENSP00000496150.1:p.Val308del
ENST00000359033.4:c.769_771del	ENSP00000351927.4:p.Val257del
ENST00000360124.9:c.540_542del	ENSP00000353241.5:p.Trp180Ter
ENST00000360608.9:c.922_924del	ENSP00000353820.5:p.Val308del
ENST00000389970.7:c.856_858del	ENSP00000374620.4:p.Val286del
ENST00000488442.1:n.1646_1648del
NM_000106.5:c.922_924del	NP_000097.3:p.Val308del
NM_001025161.2:c.769_771del	NP_001020332.2:p.Val257del
XM_011529966.1:c.922_924del	XP_011528268.1:p.Val308del
XM_011529967.1:c.922_924del	XP_011528269.1:p.Val308del
XM_011529968.1:c.922_924del	XP_011528270.1:p.Val308del
XM_011529969.1:c.778_780del	XP_011528271.1:p.Val260del
XM_011529970.1:c.769_771del	XP_011528272.1:p.Val257del
XM_011529971.1:c.778_780del	XP_011528273.1:p.Val260del
XM_011529972.1:c.843+269_844-269del	XP_011528274.1:n.843+269_844-269del
NM_000106.6:c.922_924del MANE Select	NP_000097.3:p.Val308del
NM_001025161.3:c.769_771del	NP_001020332.2:p.Val257del