Canonical Allele Identifier: CA2657033678

Gene: CYP2D6

Linked Data

• gnomAD v4: 22-42128879-AGGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128881_42128883del , CM000684.2:g.42128881_42128883del	GRCh38
NC_000022.10:g.42524883_42524885del , CM000684.1:g.42524883_42524885del	GRCh37
NC_000022.9:g.40854827_40854829del	NCBI36
NG_008376.3:g.6110_6112del
NG_008376.4:g.6929_6931del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.415_417del	ENSP00000353241.6:p.Thr139del
ENST00000645361.2:c.568_570del MANE Select	ENSP00000496150.1:p.Thr190del
ENST00000359033.4:c.415_417del	ENSP00000351927.4:p.Thr139del
ENST00000360124.9:c.235_237del	ENSP00000353241.5:p.Thr79del
ENST00000360608.9:c.568_570del	ENSP00000353820.5:p.Thr190del
ENST00000389970.7:c.502_504del	ENSP00000374620.4:p.Thr168del
ENST00000488442.1:n.1292_1294del
NM_000106.5:c.568_570del	NP_000097.3:p.Thr190del
NM_001025161.2:c.415_417del	NP_001020332.2:p.Thr139del
XM_011529966.1:c.568_570del	XP_011528268.1:p.Thr190del
XM_011529967.1:c.568_570del	XP_011528269.1:p.Thr190del
XM_011529968.1:c.568_570del	XP_011528270.1:p.Thr190del
XM_011529969.1:c.424_426del	XP_011528271.1:p.Thr142del
XM_011529970.1:c.415_417del	XP_011528272.1:p.Thr139del
XM_011529971.1:c.424_426del	XP_011528273.1:p.Thr142del
XM_011529972.1:c.568_570del	XP_011528274.1:p.Thr190del
NM_000106.6:c.568_570del MANE Select	NP_000097.3:p.Thr190del
NM_001025161.3:c.415_417del	NP_001020332.2:p.Thr139del