Canonical Allele Identifier: CA753331025

Gene: CYP2D6

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42129950A>T , CM000684.2:g.42129950A>T	GRCh38
NG_008376.3:g.5042T>A
NG_008376.4:g.5861T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.181-41T>A	ENSP00000353241.6:n.181-41T>A
ENST00000645361.2:c.181-41T>A MANE Select	ENSP00000496150.1:n.181-41T>A
ENST00000359033.4:c.181-41T>A	ENSP00000351927.4:n.181-41T>A
ENST00000360608.9:c.181-41T>A	ENSP00000353820.5:n.181-41T>A
ENST00000389970.7:c.115-41T>A	ENSP00000374620.4:n.115-41T>A
ENST00000488442.1:n.864T>A
NM_000106.5:c.181-41T>A	NP_000097.3:n.181-41T>A
NM_001025161.2:c.181-41T>A	NP_001020332.2:n.181-41T>A
XM_011529966.1:c.181-41T>A	XP_011528268.1:n.181-41T>A
XM_011529967.1:c.181-41T>A	XP_011528269.1:n.181-41T>A
XM_011529968.1:c.181-41T>A	XP_011528270.1:n.181-41T>A
XM_011529969.1:c.38-41T>A	XP_011528271.1:n.38-41T>A
XM_011529970.1:c.181-41T>A	XP_011528272.1:n.181-41T>A
XM_011529971.1:c.38-41T>A	XP_011528273.1:n.38-41T>A
XM_011529972.1:c.181-41T>A	XP_011528274.1:n.181-41T>A
XR_430455.2:n.80A>T
NM_000106.6:c.181-41T>A MANE Select	NP_000097.3:n.181-41T>A
NM_001025161.3:c.181-41T>A	NP_001020332.2:n.181-41T>A