Canonical Allele Identifier: CA2406578768

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127905_42127908delinsCCAT , CM000684.2:g.42127905_42127908delinsCCAT	GRCh38
NC_000022.10:g.42523907_42523910delinsCCAT , CM000684.1:g.42523907_42523910delinsCCAT	GRCh37
NC_000022.9:g.40853851_40853854delinsCCAT	NCBI36
NG_008376.3:g.7084_7087delinsATGG
NG_008376.4:g.7903_7906delinsATGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.717_720delinsATGG	ENSP00000353241.6:p.Gly239=
ENST00000645361.2:c.919_922delinsATGG MANE Select	ENSP00000496150.1:p.Met307=
ENST00000359033.4:c.766_769delinsATGG	ENSP00000351927.4:p.Met256=
ENST00000360124.9:c.537_540delinsATGG	ENSP00000353241.5:p.Gly179=
ENST00000360608.9:c.919_922delinsATGG	ENSP00000353820.5:p.Met307=
ENST00000389970.7:c.853_856delinsATGG	ENSP00000374620.4:p.Met285=
ENST00000488442.1:n.1643_1646delinsATGG
NM_000106.5:c.919_922delinsATGG	NP_000097.3:p.Met307=
NM_001025161.2:c.766_769delinsATGG	NP_001020332.2:p.Met256=
XM_011529966.1:c.919_922delinsATGG	XP_011528268.1:p.Met307=
XM_011529967.1:c.919_922delinsATGG	XP_011528269.1:p.Met307=
XM_011529968.1:c.919_922delinsATGG	XP_011528270.1:p.Met307=
XM_011529969.1:c.775_778delinsATGG	XP_011528271.1:p.Met259=
XM_011529970.1:c.766_769delinsATGG	XP_011528272.1:p.Met256=
XM_011529971.1:c.775_778delinsATGG	XP_011528273.1:p.Met259=
XM_011529972.1:c.843+266_843+269delinsATGG	XP_011528274.1:n.843+266_843+269delinsATGG
NM_000106.6:c.919_922delinsATGG MANE Select	NP_000097.3:p.Met307=
NM_001025161.3:c.766_769delinsATGG	NP_001020332.2:p.Met256=