Canonical Allele Identifier: CA514799790

Gene: CYP2D6

Linked Data

• MyVariant Identifiers: chr22:g.42522609T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126607T>A , CM000684.2:g.42126607T>A	GRCh38
NC_000022.10:g.42522609T>A , CM000684.1:g.42522609T>A	GRCh37
NC_000022.9:g.40852553T>A	NCBI36
NG_008376.3:g.8385A>T
NG_008376.4:g.9204A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.1259A>T	ENSP00000353241.6:n.1259A>T
ENST00000645361.2:c.1461A>T MANE Select	ENSP00000496150.1:p.Pro487=
ENST00000359033.4:c.1308A>T	ENSP00000351927.4:p.Pro436=
ENST00000360124.9:c.1079A>T	ENSP00000353241.5:n.1079A>T
ENST00000360608.9:c.1461A>T	ENSP00000353820.5:p.Pro487=
ENST00000389970.7:c.1452A>T	ENSP00000374620.4:p.Pro484=
ENST00000488442.1:n.2185A>T
NM_000106.5:c.1461A>T	NP_000097.3:p.Pro487=
NM_001025161.2:c.1308A>T	NP_001020332.2:p.Pro436=
XM_011529966.1:c.1452+9A>T	XP_011528268.1:n.1452+9A>T
XM_011529967.1:c.1452+9A>T	XP_011528269.1:n.1452+9A>T
XM_011529968.1:c.1452+9A>T	XP_011528270.1:n.1452+9A>T
XM_011529969.1:c.1308+9A>T	XP_011528271.1:n.1308+9A>T
XM_011529970.1:c.1299+9A>T	XP_011528272.1:n.1299+9A>T
XM_011529971.1:c.1317A>T	XP_011528273.1:p.Pro439=
NM_000106.6:c.1461A>T MANE Select	NP_000097.3:p.Pro487=
NM_001025161.3:c.1308A>T	NP_001020332.2:p.Pro436=