Canonical Allele Identifier: CA2819054004

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126632_42126634dup , CM000684.2:g.42126632_42126634dup	GRCh38
NC_000022.10:g.42522634_42522636dup , CM000684.1:g.42522634_42522636dup	GRCh37
NC_000022.9:g.40852578_40852580dup	NCBI36
NG_008376.3:g.8360_8362dup
NG_008376.4:g.9179_9181dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.1234_1236dup	ENSP00000353241.6:n.1234_1236dup
ENST00000645361.2:c.1436_1438dup MANE Select	ENSP00000496150.1:p.Gly479_Val480insGly
ENST00000359033.4:c.1283_1285dup	ENSP00000351927.4:p.Gly428_Val429insGly
ENST00000360124.9:c.1054_1056dup	ENSP00000353241.5:n.1054_1056dup
ENST00000360608.9:c.1436_1438dup	ENSP00000353820.5:p.Gly479_Val480insGly
ENST00000389970.7:c.1427_1429dup	ENSP00000374620.4:p.Gly476_Val477insGly
ENST00000488442.1:n.2160_2162dup
NM_000106.5:c.1436_1438dup	NP_000097.3:p.Gly479_Val480insGly
NM_001025161.2:c.1283_1285dup	NP_001020332.2:p.Gly428_Val429insGly
XM_011529966.1:c.1436_1438dup	XP_011528268.1:p.Gly479_Val480insGly
XM_011529967.1:c.1436_1438dup	XP_011528269.1:p.Gly479_Val480insGly
XM_011529968.1:c.1436_1438dup	XP_011528270.1:p.Gly479_Val480insGly
XM_011529969.1:c.1292_1294dup	XP_011528271.1:p.Gly431_Val432insGly
XM_011529970.1:c.1283_1285dup	XP_011528272.1:p.Gly428_Val429insGly
XM_011529971.1:c.1292_1294dup	XP_011528273.1:p.Gly431_Val432insGly
NM_000106.6:c.1436_1438dup MANE Select	NP_000097.3:p.Gly479_Val480insGly
NM_001025161.3:c.1283_1285dup	NP_001020332.2:p.Gly428_Val429insGly