Canonical Allele Identifier: CA514800400

Gene: CYP2D6

Linked Data

• MyVariant Identifiers: chr22:g.42523884G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127882G>T , CM000684.2:g.42127882G>T	GRCh38
NC_000022.10:g.42523884G>T , CM000684.1:g.42523884G>T	GRCh37
NC_000022.9:g.40853828G>T	NCBI36
NG_008376.3:g.7110C>A
NG_008376.4:g.7929C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.743C>A	ENSP00000353241.6:n.743C>A
ENST00000645361.2:c.945C>A MANE Select	ENSP00000496150.1:p.Ala315=
ENST00000359033.4:c.792C>A	ENSP00000351927.4:p.Ala264=
ENST00000360124.9:c.563C>A	ENSP00000353241.5:n.563C>A
ENST00000360608.9:c.945C>A	ENSP00000353820.5:p.Ala315=
ENST00000389970.7:c.879C>A	ENSP00000374620.4:p.Ala293=
ENST00000488442.1:n.1669C>A
NM_000106.5:c.945C>A	NP_000097.3:p.Ala315=
NM_001025161.2:c.792C>A	NP_001020332.2:p.Ala264=
XM_011529966.1:c.945C>A	XP_011528268.1:p.Ala315=
XM_011529967.1:c.945C>A	XP_011528269.1:p.Ala315=
XM_011529968.1:c.945C>A	XP_011528270.1:p.Ala315=
XM_011529969.1:c.801C>A	XP_011528271.1:p.Ala267=
XM_011529970.1:c.792C>A	XP_011528272.1:p.Ala264=
XM_011529971.1:c.801C>A	XP_011528273.1:p.Ala267=
XM_011529972.1:c.844-248C>A	XP_011528274.1:n.844-248C>A
NM_000106.6:c.945C>A MANE Select	NP_000097.3:p.Ala315=
NM_001025161.3:c.792C>A	NP_001020332.2:p.Ala264=