Canonical Allele Identifier: CA411773428

Gene: CYP2D6

Linked Data

• MyVariant Identifiers: chr22:g.42524277G>T (hg19) ; chr22:g.42128275G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128275G>T , CM000684.2:g.42128275G>T	GRCh38
NC_000022.10:g.42524277G>T , CM000684.1:g.42524277G>T	GRCh37
NC_000022.9:g.40854221G>T	NCBI36
NG_008376.3:g.6717C>A
NG_008376.4:g.7536C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.589C>A	ENSP00000353241.6:p.Leu197Met
ENST00000645361.2:c.742C>A MANE Select	ENSP00000496150.1:p.Leu248Met
ENST00000359033.4:c.589C>A	ENSP00000351927.4:p.Leu197Met
ENST00000360124.9:c.409C>A	ENSP00000353241.5:p.Leu137Met
ENST00000360608.9:c.742C>A	ENSP00000353820.5:p.Leu248Met
ENST00000389970.7:c.676C>A	ENSP00000374620.4:p.Leu226Met
ENST00000488442.1:n.1466C>A
NM_000106.5:c.742C>A	NP_000097.3:p.Leu248Met
NM_001025161.2:c.589C>A	NP_001020332.2:p.Leu197Met
XM_011529966.1:c.742C>A	XP_011528268.1:p.Leu248Met
XM_011529967.1:c.742C>A	XP_011528269.1:p.Leu248Met
XM_011529968.1:c.742C>A	XP_011528270.1:p.Leu248Met
XM_011529969.1:c.598C>A	XP_011528271.1:p.Leu200Met
XM_011529970.1:c.589C>A	XP_011528272.1:p.Leu197Met
XM_011529971.1:c.598C>A	XP_011528273.1:p.Leu200Met
XM_011529972.1:c.742C>A	XP_011528274.1:p.Leu248Met
NM_000106.6:c.742C>A MANE Select	NP_000097.3:p.Leu248Met
NM_001025161.3:c.589C>A	NP_001020332.2:p.Leu197Met