Canonical Allele Identifier: CA2406578322

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127313T= , CM000684.2:g.42127313T=	GRCh38
NC_000022.10:g.42523315T= , CM000684.1:g.42523315T=	GRCh37
NC_000022.9:g.40853259T=	NCBI36
NG_008376.3:g.7679A=
NG_008376.4:g.8498A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000106.6:c.1173+134A= MANE Select	NP_000097.3:n.1173+134A=
ENST00000645361.2:c.1173+134A= MANE Select	ENSP00000496150.1:n.1173+134A=
NM_000106.5:c.1173+134A=	NP_000097.3:n.1173+134A=
NM_001025161.2:c.1020+134A=	NP_001020332.2:n.1020+134A=
NM_001025161.3:c.1020+134A=	NP_001020332.2:n.1020+134A=
ENST00000359033.4:c.1020+134A=	ENSP00000351927.4:n.1020+134A=
ENST00000360124.10:c.971+134A=	ENSP00000353241.6:n.971+134A=
ENST00000360124.9:c.791+134A=	ENSP00000353241.5:n.791+134A=
ENST00000360608.9:c.1173+134A=	ENSP00000353820.5:n.1173+134A=
ENST00000389970.7:c.1164+134A=	ENSP00000374620.4:n.1164+134A=
ENST00000488442.1:n.1897+134A=
XM_011529966.1:c.1173+134A=	XP_011528268.1:n.1173+134A=
XM_011529967.1:c.1173+134A=	XP_011528269.1:n.1173+134A=
XM_011529968.1:c.1173+134A=	XP_011528270.1:n.1173+134A=
XM_011529969.1:c.1029+134A=	XP_011528271.1:n.1029+134A=
XM_011529970.1:c.1020+134A=	XP_011528272.1:n.1020+134A=
XM_011529971.1:c.1029+134A=	XP_011528273.1:n.1029+134A=