Canonical Allele Identifier: CA2406578763

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127896_42127899delinsAGGT , CM000684.2:g.42127896_42127899delinsAGGT	GRCh38
NC_000022.10:g.42523898_42523901delinsAGGT , CM000684.1:g.42523898_42523901delinsAGGT	GRCh37
NC_000022.9:g.40853842_40853845delinsAGGT	NCBI36
NG_008376.3:g.7093_7096delinsACCT
NG_008376.4:g.7912_7915delinsACCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.726_729delinsACCT	ENSP00000353241.6:n.726_729delinsACCT
ENST00000645361.2:c.928_931delinsACCT MANE Select	ENSP00000496150.1:p.Thr310=
ENST00000359033.4:c.775_778delinsACCT	ENSP00000351927.4:p.Thr259=
ENST00000360124.9:c.546_549delinsACCT	ENSP00000353241.5:n.546_549delinsACCT
ENST00000360608.9:c.928_931delinsACCT	ENSP00000353820.5:p.Thr310=
ENST00000389970.7:c.862_865delinsACCT	ENSP00000374620.4:p.Thr288=
ENST00000488442.1:n.1652_1655delinsACCT
NM_000106.5:c.928_931delinsACCT	NP_000097.3:p.Thr310=
NM_001025161.2:c.775_778delinsACCT	NP_001020332.2:p.Thr259=
XM_011529966.1:c.928_931delinsACCT	XP_011528268.1:p.Thr310=
XM_011529967.1:c.928_931delinsACCT	XP_011528269.1:p.Thr310=
XM_011529968.1:c.928_931delinsACCT	XP_011528270.1:p.Thr310=
XM_011529969.1:c.784_787delinsACCT	XP_011528271.1:p.Thr262=
XM_011529970.1:c.775_778delinsACCT	XP_011528272.1:p.Thr259=
XM_011529971.1:c.784_787delinsACCT	XP_011528273.1:p.Thr262=
XM_011529972.1:c.844-265_844-262delinsACCT	XP_011528274.1:n.844-265_844-262delinsACCT
NM_000106.6:c.928_931delinsACCT MANE Select	NP_000097.3:p.Thr310=
NM_001025161.3:c.775_778delinsACCT	NP_001020332.2:p.Thr259=