Canonical Allele Identifier: CA2406579560

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128901_42128904delinsGCTC , CM000684.2:g.42128901_42128904delinsGCTC	GRCh38
NC_000022.10:g.42524903_42524906delinsGCTC , CM000684.1:g.42524903_42524906delinsGCTC	GRCh37
NC_000022.9:g.40854847_40854850delinsGCTC	NCBI36
NG_008376.3:g.6088_6091delinsGAGC
NG_008376.4:g.6907_6910delinsGAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.393_396delinsGAGC	ENSP00000353241.6:p.Val131=
ENST00000645361.2:c.546_549delinsGAGC MANE Select	ENSP00000496150.1:p.Val182=
ENST00000359033.4:c.393_396delinsGAGC	ENSP00000351927.4:p.Val131=
ENST00000360124.9:c.213_216delinsGAGC	ENSP00000353241.5:p.Val71=
ENST00000360608.9:c.546_549delinsGAGC	ENSP00000353820.5:p.Val182=
ENST00000389970.7:c.480_483delinsGAGC	ENSP00000374620.4:p.Val160=
ENST00000488442.1:n.1270_1273delinsGAGC
NM_000106.5:c.546_549delinsGAGC	NP_000097.3:p.Val182=
NM_001025161.2:c.393_396delinsGAGC	NP_001020332.2:p.Val131=
XM_011529966.1:c.546_549delinsGAGC	XP_011528268.1:p.Val182=
XM_011529967.1:c.546_549delinsGAGC	XP_011528269.1:p.Val182=
XM_011529968.1:c.546_549delinsGAGC	XP_011528270.1:p.Val182=
XM_011529969.1:c.402_405delinsGAGC	XP_011528271.1:p.Val134=
XM_011529970.1:c.393_396delinsGAGC	XP_011528272.1:p.Val131=
XM_011529971.1:c.402_405delinsGAGC	XP_011528273.1:p.Val134=
XM_011529972.1:c.546_549delinsGAGC	XP_011528274.1:p.Val182=
NM_000106.6:c.546_549delinsGAGC MANE Select	NP_000097.3:p.Val182=
NM_001025161.3:c.393_396delinsGAGC	NP_001020332.2:p.Val131=