Canonical Allele Identifier: CA2406577803

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126600A= , CM000684.2:g.42126600A=	GRCh38
NC_000022.10:g.42522602A= , CM000684.1:g.42522602A=	GRCh37
NC_000022.9:g.40852546A=	NCBI36
NG_008376.3:g.8392T=
NG_008376.4:g.9211T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.1266T=	ENSP00000353241.6:n.1266T=
ENST00000645361.2:c.1468T= MANE Select	ENSP00000496150.1:p.Tyr490=
ENST00000359033.4:c.1315T=	ENSP00000351927.4:p.Tyr439=
ENST00000360124.9:c.1086T=	ENSP00000353241.5:n.1086T=
ENST00000360608.9:c.1468T=	ENSP00000353820.5:p.Tyr490=
ENST00000389970.7:c.1459T=	ENSP00000374620.4:p.Tyr487=
ENST00000488442.1:n.2192T=
NM_000106.5:c.1468T=	NP_000097.3:p.Tyr490=
NM_001025161.2:c.1315T=	NP_001020332.2:p.Tyr439=
XM_011529966.1:c.1452+16T=	XP_011528268.1:n.1452+16T=
XM_011529967.1:c.1452+16T=	XP_011528269.1:n.1452+16T=
XM_011529968.1:c.1452+16T=	XP_011528270.1:n.1452+16T=
XM_011529969.1:c.1308+16T=	XP_011528271.1:n.1308+16T=
XM_011529970.1:c.1299+16T=	XP_011528272.1:n.1299+16T=
XM_011529971.1:c.1324T=	XP_011528273.1:p.Tyr442=
NM_000106.6:c.1468T= MANE Select	NP_000097.3:p.Tyr490=
NM_001025161.3:c.1315T=	NP_001020332.2:p.Tyr439=