Canonical Allele Identifier: CA2406579046

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128252_42128255delinsTAGC , CM000684.2:g.42128252_42128255delinsTAGC	GRCh38
NC_000022.10:g.42524254_42524257delinsTAGC , CM000684.1:g.42524254_42524257delinsTAGC	GRCh37
NC_000022.9:g.40854198_40854201delinsTAGC	NCBI36
NG_008376.3:g.6737_6740delinsGCTA
NG_008376.4:g.7556_7559delinsGCTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.609_612delinsGCTA	ENSP00000353241.6:p.Leu203=
ENST00000645361.2:c.762_765delinsGCTA MANE Select	ENSP00000496150.1:p.Leu254=
ENST00000359033.4:c.609_612delinsGCTA	ENSP00000351927.4:p.Leu203=
ENST00000360124.9:c.429_432delinsGCTA	ENSP00000353241.5:p.Leu143=
ENST00000360608.9:c.762_765delinsGCTA	ENSP00000353820.5:p.Leu254=
ENST00000389970.7:c.696_699delinsGCTA	ENSP00000374620.4:p.Leu232=
ENST00000488442.1:n.1486_1489delinsGCTA
NM_000106.5:c.762_765delinsGCTA	NP_000097.3:p.Leu254=
NM_001025161.2:c.609_612delinsGCTA	NP_001020332.2:p.Leu203=
XM_011529966.1:c.762_765delinsGCTA	XP_011528268.1:p.Leu254=
XM_011529967.1:c.762_765delinsGCTA	XP_011528269.1:p.Leu254=
XM_011529968.1:c.762_765delinsGCTA	XP_011528270.1:p.Leu254=
XM_011529969.1:c.618_621delinsGCTA	XP_011528271.1:p.Leu206=
XM_011529970.1:c.609_612delinsGCTA	XP_011528272.1:p.Leu203=
XM_011529971.1:c.618_621delinsGCTA	XP_011528273.1:p.Leu206=
XM_011529972.1:c.762_765delinsGCTA	XP_011528274.1:p.Leu254=
NM_000106.6:c.762_765delinsGCTA MANE Select	NP_000097.3:p.Leu254=
NM_001025161.3:c.609_612delinsGCTA	NP_001020332.2:p.Leu203=