Canonical Allele Identifier: CA2738250389

Gene: CYP2D6

Linked Data

• dbSNP Id: rs2146933531

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128015_42128017del , CM000684.2:g.42128015_42128017del	GRCh38
NC_000022.10:g.42524017_42524019del , CM000684.1:g.42524017_42524019del	GRCh37
NC_000022.9:g.40853961_40853963del	NCBI36
NG_008376.3:g.6975_6977del
NG_008376.4:g.7794_7796del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.691-83_691-81del	ENSP00000353241.6:n.691-83_691-81del
ENST00000645361.2:c.844-34_844-32del MANE Select	ENSP00000496150.1:n.844-34_844-32del
ENST00000359033.4:c.691-34_691-32del	ENSP00000351927.4:n.691-34_691-32del
ENST00000360124.9:c.511-83_511-81del	ENSP00000353241.5:n.511-83_511-81del
ENST00000360608.9:c.844-34_844-32del	ENSP00000353820.5:n.844-34_844-32del
ENST00000389970.7:c.778-34_778-32del	ENSP00000374620.4:n.778-34_778-32del
ENST00000488442.1:n.1568-34_1568-32del
NM_000106.5:c.844-34_844-32del	NP_000097.3:n.844-34_844-32del
NM_001025161.2:c.691-34_691-32del	NP_001020332.2:n.691-34_691-32del
XM_011529966.1:c.844-34_844-32del	XP_011528268.1:n.844-34_844-32del
XM_011529967.1:c.844-34_844-32del	XP_011528269.1:n.844-34_844-32del
XM_011529968.1:c.844-34_844-32del	XP_011528270.1:n.844-34_844-32del
XM_011529969.1:c.700-34_700-32del	XP_011528271.1:n.700-34_700-32del
XM_011529970.1:c.691-34_691-32del	XP_011528272.1:n.691-34_691-32del
XM_011529971.1:c.700-34_700-32del	XP_011528273.1:n.700-34_700-32del
XM_011529972.1:c.843+157_843+159del	XP_011528274.1:n.843+157_843+159del
NM_000106.6:c.844-34_844-32del MANE Select	NP_000097.3:n.844-34_844-32del
NM_001025161.3:c.691-34_691-32del	NP_001020332.2:n.691-34_691-32del