Canonical Allele Identifier: CA2838446351

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126554_42126555del , CM000684.2:g.42126554_42126555del	GRCh38
NC_000022.10:g.42522556_42522557del , CM000684.1:g.42522556_42522557del	GRCh37
NC_000022.9:g.40852500_40852501del	NCBI36
NG_008376.3:g.8437_8438del
NG_008376.4:g.9256_9257del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.1311_1312del	ENSP00000353241.6:n.1311_1312del
ENST00000645361.2:c.*19_*20del MANE Select	ENSP00000496150.1:n.*19_*20del
ENST00000360124.9:c.1131_1132del	ENSP00000353241.5:n.1131_1132del
ENST00000360608.9:c.*19_*20del	ENSP00000353820.5:n.*19_*20del
ENST00000389970.7:c.*19_*20del	ENSP00000374620.4:n.*19_*20del
ENST00000488442.1:n.2237_2238del
NM_000106.5:c.*19_*20del	NP_000097.3:n.*19_*20del
NM_001025161.2:c.*19_*20del	NP_001020332.2:n.*19_*20del
XM_011529966.1:c.1452+61_1452+62del	XP_011528268.1:n.1452+61_1452+62del
XM_011529967.1:c.1452+61_1452+62del	XP_011528269.1:n.1452+61_1452+62del
XM_011529968.1:c.1452+61_1452+62del	XP_011528270.1:n.1452+61_1452+62del
XM_011529969.1:c.1308+61_1308+62del	XP_011528271.1:n.1308+61_1308+62del
XM_011529970.1:c.1299+61_1299+62del	XP_011528272.1:n.1299+61_1299+62del
XM_011529971.1:c.*19_*20del	XP_011528273.1:n.*19_*20del
NM_000106.6:c.*19_*20del MANE Select	NP_000097.3:n.*19_*20del
NM_001025161.3:c.*19_*20del	NP_001020332.2:n.*19_*20del