Canonical Allele Identifier: CA2406578786

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127926C= , CM000684.2:g.42127926C=	GRCh38
NC_000022.10:g.42523928C= , CM000684.1:g.42523928C=	GRCh37
NC_000022.9:g.40853872C=	NCBI36
NG_008376.3:g.7066G=
NG_008376.4:g.7885G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.699G=	ENSP00000353241.6:p.Leu233=
ENST00000645361.2:c.901G= MANE Select	ENSP00000496150.1:p.Asp301=
ENST00000359033.4:c.748G=	ENSP00000351927.4:p.Asp250=
ENST00000360124.9:c.519G=	ENSP00000353241.5:p.Leu173=
ENST00000360608.9:c.901G=	ENSP00000353820.5:p.Asp301=
ENST00000389970.7:c.835G=	ENSP00000374620.4:p.Asp279=
ENST00000488442.1:n.1625G=
NM_000106.5:c.901G=	NP_000097.3:p.Asp301=
NM_001025161.2:c.748G=	NP_001020332.2:p.Asp250=
XM_011529966.1:c.901G=	XP_011528268.1:p.Asp301=
XM_011529967.1:c.901G=	XP_011528269.1:p.Asp301=
XM_011529968.1:c.901G=	XP_011528270.1:p.Asp301=
XM_011529969.1:c.757G=	XP_011528271.1:p.Asp253=
XM_011529970.1:c.748G=	XP_011528272.1:p.Asp250=
XM_011529971.1:c.757G=	XP_011528273.1:p.Asp253=
XM_011529972.1:c.843+248G=	XP_011528274.1:n.843+248G=
NM_000106.6:c.901G= MANE Select	NP_000097.3:p.Asp301=
NM_001025161.3:c.748G=	NP_001020332.2:p.Asp250=