Canonical Allele Identifier: CA2657031425

Gene: CYP2D6

Linked Data

• gnomAD v4: 22-42130581-CTCTGCCGCCCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42130582_42130592del , CM000684.2:g.42130582_42130592del	GRCh38
NC_000022.10:g.42526584_42526594del , CM000684.1:g.42526584_42526594del	GRCh37
NC_000022.9:g.40856528_40856538del	NCBI36
NG_008376.3:g.4400_4410del
NG_008376.4:g.5219_5229del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.180+20_180+30del	ENSP00000353241.6:n.180+20_180+30del
ENST00000645361.2:c.180+20_180+30del MANE Select	ENSP00000496150.1:n.180+20_180+30del
ENST00000359033.4:c.180+20_180+30del	ENSP00000351927.4:n.180+20_180+30del
ENST00000360608.9:c.180+20_180+30del	ENSP00000353820.5:n.180+20_180+30del
ENST00000389970.7:c.114+20_114+30del	ENSP00000374620.4:n.114+20_114+30del
ENST00000488442.1:n.222_232del
NM_000106.5:c.180+20_180+30del	NP_000097.3:n.180+20_180+30del
NM_001025161.2:c.180+20_180+30del	NP_001020332.2:n.180+20_180+30del
XM_011529966.1:c.180+20_180+30del	XP_011528268.1:n.180+20_180+30del
XM_011529967.1:c.180+20_180+30del	XP_011528269.1:n.180+20_180+30del
XM_011529968.1:c.180+20_180+30del	XP_011528270.1:n.180+20_180+30del
XM_011529969.1:c.38-683_38-673del	XP_011528271.1:n.38-683_38-673del
XM_011529970.1:c.180+20_180+30del	XP_011528272.1:n.180+20_180+30del
XM_011529971.1:c.38-683_38-673del	XP_011528273.1:n.38-683_38-673del
XM_011529972.1:c.180+20_180+30del	XP_011528274.1:n.180+20_180+30del
XR_430455.2:n.222_232del
NM_000106.6:c.180+20_180+30del MANE Select	NP_000097.3:n.180+20_180+30del
XR_002958749.1:n.169_179del
NM_001025161.3:c.180+20_180+30del	NP_001020332.2:n.180+20_180+30del