Canonical Allele Identifier: CA2695230936

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127915dup , CM000684.2:g.42127915dup	GRCh38
NC_000022.10:g.42523917dup , CM000684.1:g.42523917dup	GRCh37
NC_000022.9:g.40853861dup	NCBI36
NG_008376.3:g.7077dup
NG_008376.4:g.7896dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.710dup	ENSP00000353241.6:p.Pro238AlafsTer?
ENST00000645361.2:c.912dup MANE Select	ENSP00000496150.1:p.Ala305CysfsTer?
ENST00000359033.4:c.759dup	ENSP00000351927.4:p.Ala254CysfsTer?
ENST00000360124.9:c.530dup	ENSP00000353241.5:p.Pro178AlafsTer?
ENST00000360608.9:c.912dup	ENSP00000353820.5:p.Ala305CysfsTer?
ENST00000389970.7:c.846dup	ENSP00000374620.4:p.Ala283CysfsTer?
ENST00000488442.1:n.1636dup
NM_000106.5:c.912dup	NP_000097.3:p.Ala305CysfsTer?
NM_001025161.2:c.759dup	NP_001020332.2:p.Ala254CysfsTer?
XM_011529966.1:c.912dup	XP_011528268.1:p.Ala305CysfsTer?
XM_011529967.1:c.912dup	XP_011528269.1:p.Ala305CysfsTer?
XM_011529968.1:c.912dup	XP_011528270.1:p.Ala305CysfsTer?
XM_011529969.1:c.768dup	XP_011528271.1:p.Ala257CysfsTer?
XM_011529970.1:c.759dup	XP_011528272.1:p.Ala254CysfsTer?
XM_011529971.1:c.768dup	XP_011528273.1:p.Ala257CysfsTer?
XM_011529972.1:c.843+259dup	XP_011528274.1:n.843+259dup
NM_000106.6:c.912dup MANE Select	NP_000097.3:p.Ala305CysfsTer?
NM_001025161.3:c.759dup	NP_001020332.2:p.Ala254CysfsTer?