Canonical Allele Identifier: CA2406579785

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42129182_42129183delinsAC , CM000684.2:g.42129182_42129183delinsAC	GRCh38
NC_000022.10:g.42525184_42525185delinsAC , CM000684.1:g.42525184_42525185delinsAC	GRCh37
NC_000022.9:g.40855128_40855129delinsAC	NCBI36
NG_008376.3:g.5809_5810delinsGT
NG_008376.4:g.6628_6629delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.353-239_353-238delinsGT	ENSP00000353241.6:n.353-239_353-238delinsGT
ENST00000645361.2:c.355_356delinsGT MANE Select	ENSP00000496150.1:p.Val119=
ENST00000359033.4:c.353-239_353-238delinsGT	ENSP00000351927.4:n.353-239_353-238delinsGT
ENST00000360124.9:c.173-239_173-238delinsGT	ENSP00000353241.5:n.173-239_173-238delinsGT
ENST00000360608.9:c.355_356delinsGT	ENSP00000353820.5:p.Val119=
ENST00000389970.7:c.289_290delinsGT	ENSP00000374620.4:p.Val97=
ENST00000488442.1:n.1079_1080delinsGT
NM_000106.5:c.355_356delinsGT	NP_000097.3:p.Val119=
NM_001025161.2:c.353-239_353-238delinsGT	NP_001020332.2:n.353-239_353-238delinsGT
XM_011529966.1:c.355_356delinsGT	XP_011528268.1:p.Val119=
XM_011529967.1:c.355_356delinsGT	XP_011528269.1:p.Val119=
XM_011529968.1:c.355_356delinsGT	XP_011528270.1:p.Val119=
XM_011529969.1:c.212_213delinsGT	XP_011528271.1:p.Gly71=
XM_011529970.1:c.353-239_353-238delinsGT	XP_011528272.1:n.353-239_353-238delinsGT
XM_011529971.1:c.212_213delinsGT	XP_011528273.1:p.Gly71=
XM_011529972.1:c.355_356delinsGT	XP_011528274.1:p.Val119=
NM_000106.6:c.355_356delinsGT MANE Select	NP_000097.3:p.Val119=
NM_001025161.3:c.353-239_353-238delinsGT	NP_001020332.2:n.353-239_353-238delinsGT