Canonical Allele Identifier: CA2406578909

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128093_42128094delinsAC , CM000684.2:g.42128093_42128094delinsAC	GRCh38
NC_000022.10:g.42524095_42524096delinsAC , CM000684.1:g.42524095_42524096delinsAC	GRCh37
NC_000022.9:g.40854039_40854040delinsAC	NCBI36
NG_008376.3:g.6898_6899delinsGT
NG_008376.4:g.7717_7718delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.690+80_690+81delinsGT	ENSP00000353241.6:n.690+80_690+81delinsGT...
ENST00000645361.2:c.843+80_843+81delinsGT MANE Select	ENSP00000496150.1:n.843+80_843+81delinsGT...
ENST00000359033.4:c.690+80_690+81delinsGT	ENSP00000351927.4:n.690+80_690+81delinsGT...
ENST00000360124.9:c.510+80_510+81delinsGT	ENSP00000353241.5:n.510+80_510+81delinsGT...
ENST00000360608.9:c.843+80_843+81delinsGT	ENSP00000353820.5:n.843+80_843+81delinsGT...
ENST00000389970.7:c.777+80_777+81delinsGT	ENSP00000374620.4:n.777+80_777+81delinsGT...
ENST00000488442.1:n.1567+80_1567+81delinsGT
NM_000106.5:c.843+80_843+81delinsGT	NP_000097.3:n.843+80_843+81delinsGT
NM_001025161.2:c.690+80_690+81delinsGT	NP_001020332.2:n.690+80_690+81delinsGT
XM_011529966.1:c.843+80_843+81delinsGT	XP_011528268.1:n.843+80_843+81delinsGT
XM_011529967.1:c.843+80_843+81delinsGT	XP_011528269.1:n.843+80_843+81delinsGT
XM_011529968.1:c.843+80_843+81delinsGT	XP_011528270.1:n.843+80_843+81delinsGT
XM_011529969.1:c.699+80_699+81delinsGT	XP_011528271.1:n.699+80_699+81delinsGT
XM_011529970.1:c.690+80_690+81delinsGT	XP_011528272.1:n.690+80_690+81delinsGT
XM_011529971.1:c.699+80_699+81delinsGT	XP_011528273.1:n.699+80_699+81delinsGT
XM_011529972.1:c.843+80_843+81delinsGT	XP_011528274.1:n.843+80_843+81delinsGT
NM_000106.6:c.843+80_843+81delinsGT MANE Select	NP_000097.3:n.843+80_843+81delinsGT
NM_001025161.3:c.690+80_690+81delinsGT	NP_001020332.2:n.690+80_690+81delinsGT