Canonical Allele Identifier: CA639828031

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1237764592
• gnomAD v2: 22-42523677-GGGTCCGGCCCT-G
• gnomAD v3: 22-42127675-GGGTCCGGCCCT-G
• gnomAD v4: 22-42127675-GGGTCCGGCCCT-G
• MyVariant Identifiers: chr22:g.42523678_42523688del (hg19) ; chr22:g.42127676_42127686del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127677_42127687del , CM000684.2:g.42127677_42127687del	GRCh38
NC_000022.10:g.42523679_42523689del , CM000684.1:g.42523679_42523689del	GRCh37
NC_000022.9:g.40853623_40853633del	NCBI36
NG_008376.3:g.7306_7316del
NG_008376.4:g.8125_8135del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.784-52_784-42del	ENSP00000353241.6:n.784-52_784-42del
ENST00000645361.2:c.986-52_986-42del MANE Select	ENSP00000496150.1:n.986-52_986-42del
ENST00000359033.4:c.833-52_833-42del	ENSP00000351927.4:n.833-52_833-42del
ENST00000360124.9:c.604-52_604-42del	ENSP00000353241.5:n.604-52_604-42del
ENST00000360608.9:c.986-52_986-42del	ENSP00000353820.5:n.986-52_986-42del
ENST00000389970.7:c.949-24_949-14del	ENSP00000374620.4:n.949-24_949-14del
ENST00000488442.1:n.1710-52_1710-42del
NM_000106.5:c.986-52_986-42del	NP_000097.3:n.986-52_986-42del
NM_001025161.2:c.833-52_833-42del	NP_001020332.2:n.833-52_833-42del
XM_011529966.1:c.986-52_986-42del	XP_011528268.1:n.986-52_986-42del
XM_011529967.1:c.986-52_986-42del	XP_011528269.1:n.986-52_986-42del
XM_011529968.1:c.986-52_986-42del	XP_011528270.1:n.986-52_986-42del
XM_011529969.1:c.842-52_842-42del	XP_011528271.1:n.842-52_842-42del
XM_011529970.1:c.833-52_833-42del	XP_011528272.1:n.833-52_833-42del
XM_011529971.1:c.842-52_842-42del	XP_011528273.1:n.842-52_842-42del
XM_011529972.1:c.844-52_844-42del	XP_011528274.1:n.844-52_844-42del
NM_000106.6:c.986-52_986-42del MANE Select	NP_000097.3:n.986-52_986-42del
NM_001025161.3:c.833-52_833-42del	NP_001020332.2:n.833-52_833-42del