Canonical Allele Identifier: CA324666203

Gene: CYP2D6

Linked Data

• dbSNP Id: rs879550940

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127855del , CM000684.2:g.42127855del	GRCh38
NC_000022.10:g.42523857del , CM000684.1:g.42523857del	GRCh37
NC_000022.9:g.40853801del	NCBI36
NG_008376.3:g.7137del
NG_008376.4:g.7956del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.770del	ENSP00000353241.6:n.770del
ENST00000645361.2:c.972del MANE Select	ENSP00000496150.1:p.Pro325ArgfsTer14
ENST00000359033.4:c.819del	ENSP00000351927.4:p.Pro274ArgfsTer14
ENST00000360124.9:c.590del	ENSP00000353241.5:n.590del
ENST00000360608.9:c.972del	ENSP00000353820.5:p.Pro325ArgfsTer14
ENST00000389970.7:c.906del	ENSP00000374620.4:p.Pro303ArgfsTer?
ENST00000488442.1:n.1696del
NM_000106.5:c.972del	NP_000097.3:p.Pro325ArgfsTer14
NM_001025161.2:c.819del	NP_001020332.2:p.Pro274ArgfsTer14
XM_011529966.1:c.972del	XP_011528268.1:p.Pro325ArgfsTer14
XM_011529967.1:c.972del	XP_011528269.1:p.Pro325ArgfsTer14
XM_011529968.1:c.972del	XP_011528270.1:p.Pro325ArgfsTer14
XM_011529969.1:c.828del	XP_011528271.1:p.Pro277ArgfsTer14
XM_011529970.1:c.819del	XP_011528272.1:p.Pro274ArgfsTer14
XM_011529971.1:c.828del	XP_011528273.1:p.Pro277ArgfsTer14
XM_011529972.1:c.844-221del	XP_011528274.1:n.844-221del
NM_000106.6:c.972del MANE Select	NP_000097.3:p.Pro325ArgfsTer14
NM_001025161.3:c.819del	NP_001020332.2:p.Pro274ArgfsTer14