Canonical Allele Identifier: CA2819054003

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126532_42126533del , CM000684.2:g.42126532_42126533del	GRCh38
NC_000022.10:g.42522534_42522535del , CM000684.1:g.42522534_42522535del	GRCh37
NC_000022.9:g.40852478_40852479del	NCBI36
NG_008376.3:g.8461_8462del
NG_008376.4:g.9280_9281del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.1335_1336del	ENSP00000353241.6:n.1335_1336del
ENST00000645361.2:c.*43_*44del MANE Select	ENSP00000496150.1:n.*43_*44del
ENST00000360124.9:c.1155_1156del	ENSP00000353241.5:n.1155_1156del
ENST00000360608.9:c.*43_*44del	ENSP00000353820.5:n.*43_*44del
ENST00000389970.7:c.*43_*44del	ENSP00000374620.4:n.*43_*44del
NM_000106.5:c.*43_*44del	NP_000097.3:n.*43_*44del
NM_001025161.2:c.*43_*44del	NP_001020332.2:n.*43_*44del
XM_011529966.1:c.1452+85_1452+86del	XP_011528268.1:n.1452+85_1452+86del
XM_011529967.1:c.1452+85_1452+86del	XP_011528269.1:n.1452+85_1452+86del
XM_011529968.1:c.1452+85_1452+86del	XP_011528270.1:n.1452+85_1452+86del
XM_011529969.1:c.1308+85_1308+86del	XP_011528271.1:n.1308+85_1308+86del
XM_011529970.1:c.1299+85_1299+86del	XP_011528272.1:n.1299+85_1299+86del
XM_011529971.1:c.*43_*44del	XP_011528273.1:n.*43_*44del
NM_000106.6:c.*43_*44del MANE Select	NP_000097.3:n.*43_*44del
NM_001025161.3:c.*43_*44del	NP_001020332.2:n.*43_*44del