Canonical Allele Identifier: CA2406577813

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126617_42126618delinsAG , CM000684.2:g.42126617_42126618delinsAG	GRCh38
NC_000022.10:g.42522619_42522620delinsAG , CM000684.1:g.42522619_42522620delinsAG	GRCh37
NC_000022.9:g.40852563_40852564delinsAG	NCBI36
NG_008376.3:g.8374_8375delinsCT
NG_008376.4:g.9193_9194delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.1248_1249delinsCT	ENSP00000353241.6:n.1248_1249delinsCT
ENST00000645361.2:c.1450_1451delinsCT MANE Select	ENSP00000496150.1:p.Leu484=
ENST00000359033.4:c.1297_1298delinsCT	ENSP00000351927.4:p.Leu433=
ENST00000360124.9:c.1068_1069delinsCT	ENSP00000353241.5:n.1068_1069delinsCT
ENST00000360608.9:c.1450_1451delinsCT	ENSP00000353820.5:p.Leu484=
ENST00000389970.7:c.1441_1442delinsCT	ENSP00000374620.4:p.Leu481=
ENST00000488442.1:n.2174_2175delinsCT
NM_000106.5:c.1450_1451delinsCT	NP_000097.3:p.Leu484=
NM_001025161.2:c.1297_1298delinsCT	NP_001020332.2:p.Leu433=
XM_011529966.1:c.1450_1451delinsCT	XP_011528268.1:p.Leu484=
XM_011529967.1:c.1450_1451delinsCT	XP_011528269.1:p.Leu484=
XM_011529968.1:c.1450_1451delinsCT	XP_011528270.1:p.Leu484=
XM_011529969.1:c.1306_1307delinsCT	XP_011528271.1:p.Leu436=
XM_011529970.1:c.1297_1298delinsCT	XP_011528272.1:p.Leu433=
XM_011529971.1:c.1306_1307delinsCT	XP_011528273.1:p.Leu436=
NM_000106.6:c.1450_1451delinsCT MANE Select	NP_000097.3:p.Leu484=
NM_001025161.3:c.1297_1298delinsCT	NP_001020332.2:p.Leu433=