Canonical Allele Identifier: CA2406577762

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126532A= , CM000684.2:g.42126532A=	GRCh38
NC_000022.10:g.42522534A= , CM000684.1:g.42522534A=	GRCh37
NC_000022.9:g.40852478A=	NCBI36
NG_008376.3:g.8460T=
NG_008376.4:g.9279T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.1334T=	ENSP00000353241.6:n.1334T=
ENST00000645361.2:c.*42T= MANE Select	ENSP00000496150.1:n.*42T=
ENST00000360124.9:c.1154T=	ENSP00000353241.5:n.1154T=
ENST00000360608.9:c.*42T=	ENSP00000353820.5:n.*42T=
ENST00000389970.7:c.*42T=	ENSP00000374620.4:n.*42T=
NM_000106.5:c.*42T=	NP_000097.3:n.*42T=
NM_001025161.2:c.*42T=	NP_001020332.2:n.*42T=
XM_011529966.1:c.1452+84T=	XP_011528268.1:n.1452+84T=
XM_011529967.1:c.1452+84T=	XP_011528269.1:n.1452+84T=
XM_011529968.1:c.1452+84T=	XP_011528270.1:n.1452+84T=
XM_011529969.1:c.1308+84T=	XP_011528271.1:n.1308+84T=
XM_011529970.1:c.1299+84T=	XP_011528272.1:n.1299+84T=
XM_011529971.1:c.*42T=	XP_011528273.1:n.*42T=
NM_000106.6:c.*42T= MANE Select	NP_000097.3:n.*42T=
NM_001025161.3:c.*42T=	NP_001020332.2:n.*42T=