Canonical Allele Identifier: CA411773293

Gene: CYP2D6

Linked Data

• MyVariant Identifiers: chr22:g.42128243del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128243del , CM000684.2:g.42128243del	GRCh38
NC_000022.10:g.42524245del , CM000684.1:g.42524245del	GRCh37
NC_000022.9:g.40854189del	NCBI36
NG_008376.3:g.6749del
NG_008376.4:g.7568del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.621del	ENSP00000353241.6:p.His207GlnfsTer3
ENST00000645361.2:c.774del MANE Select	ENSP00000496150.1:p.His258GlnfsTer3
ENST00000359033.4:c.621del	ENSP00000351927.4:p.His207GlnfsTer3
ENST00000360124.9:c.441del	ENSP00000353241.5:p.His147GlnfsTer3
ENST00000360608.9:c.774del	ENSP00000353820.5:p.His258GlnfsTer3
ENST00000389970.7:c.708del	ENSP00000374620.4:p.His236GlnfsTer3
ENST00000488442.1:n.1498del
NM_000106.5:c.774del	NP_000097.3:p.His258GlnfsTer3
NM_001025161.2:c.621del	NP_001020332.2:p.His207GlnfsTer3
XM_011529966.1:c.774del	XP_011528268.1:p.His258GlnfsTer3
XM_011529967.1:c.774del	XP_011528269.1:p.His258GlnfsTer3
XM_011529968.1:c.774del	XP_011528270.1:p.His258GlnfsTer3
XM_011529969.1:c.630del	XP_011528271.1:p.His210GlnfsTer3
XM_011529970.1:c.621del	XP_011528272.1:p.His207GlnfsTer3
XM_011529971.1:c.630del	XP_011528273.1:p.His210GlnfsTer3
XM_011529972.1:c.774del	XP_011528274.1:p.His258GlnfsTer3
NM_000106.6:c.774del MANE Select	NP_000097.3:p.His258GlnfsTer3
NM_001025161.3:c.621del	NP_001020332.2:p.His207GlnfsTer3