Canonical Allele Identifier: CA2406578503

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127537A= , CM000684.2:g.42127537A=	GRCh38
NC_000022.10:g.42523539A= , CM000684.1:g.42523539A=	GRCh37
NC_000022.9:g.40853483A=	NCBI36
NG_008376.3:g.7455T=
NG_008376.4:g.8274T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000106.6:c.1083T= MANE Select	NP_000097.3:p.His361=
ENST00000645361.2:c.1083T= MANE Select	ENSP00000496150.1:p.His361=
NM_000106.5:c.1083T=	NP_000097.3:p.His361=
NM_001025161.2:c.930T=	NP_001020332.2:p.His310=
NM_001025161.3:c.930T=	NP_001020332.2:p.His310=
ENST00000359033.4:c.930T=	ENSP00000351927.4:p.His310=
ENST00000360124.10:c.881T=	ENSP00000353241.6:n.881T=
ENST00000360124.9:c.701T=	ENSP00000353241.5:n.701T=
ENST00000360608.9:c.1083T=	ENSP00000353820.5:p.His361=
ENST00000389970.7:c.1074T=	ENSP00000374620.4:p.His358=
ENST00000488442.1:n.1807T=
XM_011529966.1:c.1083T=	XP_011528268.1:p.His361=
XM_011529967.1:c.1083T=	XP_011528269.1:p.His361=
XM_011529968.1:c.1083T=	XP_011528270.1:p.His361=
XM_011529969.1:c.939T=	XP_011528271.1:p.His313=
XM_011529970.1:c.930T=	XP_011528272.1:p.His310=
XM_011529971.1:c.939T=	XP_011528273.1:p.His313=
XM_011529972.1:c.*68T=	XP_011528274.1:n.*68T=