Canonical Allele Identifier: CA915951402

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126819A>G , CM000684.2:g.42126819A>G	GRCh38
NC_000022.10:g.42522821A>G , CM000684.1:g.42522821A>G	GRCh37
NC_000022.9:g.40852765A>G	NCBI36
NG_008376.3:g.8173T>C
NG_008376.4:g.8992T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.1113+32T>C	ENSP00000353241.6:n.1113+32T>C
ENST00000645361.2:c.1315+32T>C MANE Select	ENSP00000496150.1:n.1315+32T>C
ENST00000359033.4:c.1162+32T>C	ENSP00000351927.4:n.1162+32T>C
ENST00000360124.9:c.933+32T>C	ENSP00000353241.5:n.933+32T>C
ENST00000360608.9:c.1315+32T>C	ENSP00000353820.5:n.1315+32T>C
ENST00000389970.7:c.1306+32T>C	ENSP00000374620.4:n.1306+32T>C
ENST00000488442.1:n.2039+32T>C
NM_000106.5:c.1315+32T>C	NP_000097.3:n.1315+32T>C
NM_001025161.2:c.1162+32T>C	NP_001020332.2:n.1162+32T>C
XM_011529966.1:c.1315+32T>C	XP_011528268.1:n.1315+32T>C
XM_011529967.1:c.1315+32T>C	XP_011528269.1:n.1315+32T>C
XM_011529968.1:c.1315+32T>C	XP_011528270.1:n.1315+32T>C
XM_011529969.1:c.1171+32T>C	XP_011528271.1:n.1171+32T>C
XM_011529970.1:c.1162+32T>C	XP_011528272.1:n.1162+32T>C
XM_011529971.1:c.1171+32T>C	XP_011528273.1:n.1171+32T>C
NM_000106.6:c.1315+32T>C MANE Select	NP_000097.3:n.1315+32T>C
NM_001025161.3:c.1162+32T>C	NP_001020332.2:n.1162+32T>C