Canonical Allele Identifier: CA2512099197

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126560_42126562dup , CM000684.2:g.42126560_42126562dup	GRCh38
NC_000022.10:g.42522562_42522564dup , CM000684.1:g.42522562_42522564dup	GRCh37
NC_000022.9:g.40852506_40852508dup	NCBI36
NG_008376.3:g.8431_8433dup
NG_008376.4:g.9250_9252dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.1305_1307dup	ENSP00000353241.6:n.1305_1307dup
ENST00000645361.2:c.*13_*15dup MANE Select	ENSP00000496150.1:n.*13_*15dup
ENST00000359033.4:c.*13_*15dup	ENSP00000351927.4:n.*13_*15dup
ENST00000360124.9:c.1125_1127dup	ENSP00000353241.5:n.1125_1127dup
ENST00000360608.9:c.*13_*15dup	ENSP00000353820.5:n.*13_*15dup
ENST00000389970.7:c.*13_*15dup	ENSP00000374620.4:n.*13_*15dup
ENST00000488442.1:n.2231_2233dup
NM_000106.5:c.*13_*15dup	NP_000097.3:n.*13_*15dup
NM_001025161.2:c.*13_*15dup	NP_001020332.2:n.*13_*15dup
XM_011529966.1:c.1452+55_1452+57dup	XP_011528268.1:n.1452+55_1452+57dup
XM_011529967.1:c.1452+55_1452+57dup	XP_011528269.1:n.1452+55_1452+57dup
XM_011529968.1:c.1452+55_1452+57dup	XP_011528270.1:n.1452+55_1452+57dup
XM_011529969.1:c.1308+55_1308+57dup	XP_011528271.1:n.1308+55_1308+57dup
XM_011529970.1:c.1299+55_1299+57dup	XP_011528272.1:n.1299+55_1299+57dup
XM_011529971.1:c.*13_*15dup	XP_011528273.1:n.*13_*15dup
NM_000106.6:c.*13_*15dup MANE Select	NP_000097.3:n.*13_*15dup
NM_001025161.3:c.*13_*15dup	NP_001020332.2:n.*13_*15dup