Canonical Allele Identifier: CA324664605

Gene: CYP2D6

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126663G>T , CM000684.2:g.42126663G>T	GRCh38
NC_000022.10:g.42522665G>T , CM000684.1:g.42522665G>T	GRCh37
NC_000022.9:g.40852609G>T	NCBI36
NG_008376.3:g.8329C>A
NG_008376.4:g.9148C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.1203C>A	ENSP00000353241.6:n.1203C>A
ENST00000645361.2:c.1405C>A MANE Select	ENSP00000496150.1:p.Pro469Thr
ENST00000359033.4:c.1252C>A	ENSP00000351927.4:p.Pro418Thr
ENST00000360124.9:c.1023C>A	ENSP00000353241.5:n.1023C>A
ENST00000360608.9:c.1405C>A	ENSP00000353820.5:p.Pro469Thr
ENST00000389970.7:c.1396C>A	ENSP00000374620.4:p.Pro466Thr
ENST00000488442.1:n.2129C>A
NM_000106.5:c.1405C>A	NP_000097.3:p.Pro469Thr
NM_001025161.2:c.1252C>A	NP_001020332.2:p.Pro418Thr
XM_011529966.1:c.1405C>A	XP_011528268.1:p.Pro469Thr
XM_011529967.1:c.1405C>A	XP_011528269.1:p.Pro469Thr
XM_011529968.1:c.1405C>A	XP_011528270.1:p.Pro469Thr
XM_011529969.1:c.1261C>A	XP_011528271.1:p.Pro421Thr
XM_011529970.1:c.1252C>A	XP_011528272.1:p.Pro418Thr
XM_011529971.1:c.1261C>A	XP_011528273.1:p.Pro421Thr
NM_000106.6:c.1405C>A MANE Select	NP_000097.3:p.Pro469Thr
NM_001025161.3:c.1252C>A	NP_001020332.2:p.Pro418Thr