Canonical Allele Identifier: CA2406579680

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42129042T= , CM000684.2:g.42129042T=	GRCh38
NC_000022.10:g.42525044T= , CM000684.1:g.42525044T=	GRCh37
NC_000022.9:g.40854988T=	NCBI36
NG_008376.3:g.5950A=
NG_008376.4:g.6769A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000106.6:c.496A= MANE Select	NP_000097.3:p.Asn166=
ENST00000645361.2:c.496A= MANE Select	ENSP00000496150.1:p.Asn166=
NM_000106.5:c.496A=	NP_000097.3:p.Asn166=
NM_001025161.2:c.353-98A=	NP_001020332.2:n.353-98A=
NM_001025161.3:c.353-98A=	NP_001020332.2:n.353-98A=
ENST00000359033.4:c.353-98A=	ENSP00000351927.4:n.353-98A=
ENST00000360124.10:c.353-98A=	ENSP00000353241.6:n.353-98A=
ENST00000360124.9:c.173-98A=	ENSP00000353241.5:n.173-98A=
ENST00000360608.9:c.496A=	ENSP00000353820.5:p.Asn166=
ENST00000389970.7:c.430A=	ENSP00000374620.4:p.Asn144=
ENST00000488442.1:n.1220A=
XM_011529966.1:c.496A=	XP_011528268.1:p.Asn166=
XM_011529967.1:c.496A=	XP_011528269.1:p.Asn166=
XM_011529968.1:c.496A=	XP_011528270.1:p.Asn166=
XM_011529969.1:c.353A=	XP_011528271.1:p.Gln118=
XM_011529970.1:c.353-98A=	XP_011528272.1:n.353-98A=
XM_011529971.1:c.353A=	XP_011528273.1:p.Gln118=
XM_011529972.1:c.496A=	XP_011528274.1:p.Asn166=