Canonical Allele Identifier: CA2406579578

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128925G= , CM000684.2:g.42128925G=	GRCh38
NC_000022.10:g.42524927G= , CM000684.1:g.42524927G=	GRCh37
NC_000022.9:g.40854871G=	NCBI36
NG_008376.3:g.6067C=
NG_008376.4:g.6886C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.372C=	ENSP00000353241.6:p.Asn124=
ENST00000645361.2:c.525C= MANE Select	ENSP00000496150.1:p.Asn175=
ENST00000359033.4:c.372C=	ENSP00000351927.4:p.Asn124=
ENST00000360124.9:c.192C=	ENSP00000353241.5:p.Asn64=
ENST00000360608.9:c.525C=	ENSP00000353820.5:p.Asn175=
ENST00000389970.7:c.459C=	ENSP00000374620.4:p.Asn153=
ENST00000488442.1:n.1249C=
NM_000106.5:c.525C=	NP_000097.3:p.Asn175=
NM_001025161.2:c.372C=	NP_001020332.2:p.Asn124=
XM_011529966.1:c.525C=	XP_011528268.1:p.Asn175=
XM_011529967.1:c.525C=	XP_011528269.1:p.Asn175=
XM_011529968.1:c.525C=	XP_011528270.1:p.Asn175=
XM_011529969.1:c.381C=	XP_011528271.1:p.Asn127=
XM_011529970.1:c.372C=	XP_011528272.1:p.Asn124=
XM_011529971.1:c.381C=	XP_011528273.1:p.Asn127=
XM_011529972.1:c.525C=	XP_011528274.1:p.Asn175=
NM_000106.6:c.525C= MANE Select	NP_000097.3:p.Asn175=
NM_001025161.3:c.372C=	NP_001020332.2:p.Asn124=