Canonical Allele Identifier: CA514800243

Gene: CYP2D6

Linked Data

• MyVariant Identifiers: chr22:g.42523944C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127942C>A , CM000684.2:g.42127942C>A	GRCh38
NC_000022.10:g.42523944C>A , CM000684.1:g.42523944C>A	GRCh37
NC_000022.9:g.40853888C>A	NCBI36
NG_008376.3:g.7050G>T
NG_008376.4:g.7869G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.691-8G>T	ENSP00000353241.6:n.691-8G>T
ENST00000645361.2:c.885G>T MANE Select	ENSP00000496150.1:p.Leu295=
ENST00000359033.4:c.732G>T	ENSP00000351927.4:p.Leu244=
ENST00000360124.9:c.511-8G>T	ENSP00000353241.5:n.511-8G>T
ENST00000360608.9:c.885G>T	ENSP00000353820.5:p.Leu295=
ENST00000389970.7:c.819G>T	ENSP00000374620.4:p.Leu273=
ENST00000488442.1:n.1609G>T
NM_000106.5:c.885G>T	NP_000097.3:p.Leu295=
NM_001025161.2:c.732G>T	NP_001020332.2:p.Leu244=
XM_011529966.1:c.885G>T	XP_011528268.1:p.Leu295=
XM_011529967.1:c.885G>T	XP_011528269.1:p.Leu295=
XM_011529968.1:c.885G>T	XP_011528270.1:p.Leu295=
XM_011529969.1:c.741G>T	XP_011528271.1:p.Leu247=
XM_011529970.1:c.732G>T	XP_011528272.1:p.Leu244=
XM_011529971.1:c.741G>T	XP_011528273.1:p.Leu247=
XM_011529972.1:c.843+232G>T	XP_011528274.1:n.843+232G>T
NM_000106.6:c.885G>T MANE Select	NP_000097.3:p.Leu295=
NM_001025161.3:c.732G>T	NP_001020332.2:p.Leu244=