Canonical Allele Identifier: CA411773561

Gene: CYP2D6

Linked Data

• COSMIC: COSM1566432 ; COSM1566433
• MyVariant Identifiers: chr22:g.42524322T>A (hg19) ; chr22:g.42128320T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128320T>A , CM000684.2:g.42128320T>A	GRCh38
NC_000022.10:g.42524322T>A , CM000684.1:g.42524322T>A	GRCh37
NC_000022.9:g.40854266T>A	NCBI36
NG_008376.3:g.6672A>T
NG_008376.4:g.7491A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.544A>T	ENSP00000353241.6:p.Ile182Phe
ENST00000645361.2:c.697A>T MANE Select	ENSP00000496150.1:p.Ile233Phe
ENST00000359033.4:c.544A>T	ENSP00000351927.4:p.Ile182Phe
ENST00000360124.9:c.364A>T	ENSP00000353241.5:p.Ile122Phe
ENST00000360608.9:c.697A>T	ENSP00000353820.5:p.Ile233Phe
ENST00000389970.7:c.631A>T	ENSP00000374620.4:p.Ile211Phe
ENST00000488442.1:n.1421A>T
NM_000106.5:c.697A>T	NP_000097.3:p.Ile233Phe
NM_001025161.2:c.544A>T	NP_001020332.2:p.Ile182Phe
XM_011529966.1:c.697A>T	XP_011528268.1:p.Ile233Phe
XM_011529967.1:c.697A>T	XP_011528269.1:p.Ile233Phe
XM_011529968.1:c.697A>T	XP_011528270.1:p.Ile233Phe
XM_011529969.1:c.553A>T	XP_011528271.1:p.Ile185Phe
XM_011529970.1:c.544A>T	XP_011528272.1:p.Ile182Phe
XM_011529971.1:c.553A>T	XP_011528273.1:p.Ile185Phe
XM_011529972.1:c.697A>T	XP_011528274.1:p.Ile233Phe
NM_000106.6:c.697A>T MANE Select	NP_000097.3:p.Ile233Phe
NM_001025161.3:c.544A>T	NP_001020332.2:p.Ile182Phe