Canonical Allele Identifier: CA2406578805
Gene: CYP2D6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42127953C= , CM000684.2:g.42127953C= GRCh38
NC_000022.10:g.42523955C= , CM000684.1:g.42523955C= GRCh37
NC_000022.9:g.40853899C= NCBI36
NG_008376.3:g.7039G=
NG_008376.4:g.7858G=

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.691-19G= ENSP00000353241.6:n.691-19G=
ENST00000645361.2:c.874G= MANE Select ENSP00000496150.1:p.Asp292=
ENST00000359033.4:c.721G= ENSP00000351927.4:p.Asp241=
ENST00000360124.9:c.511-19G= ENSP00000353241.5:n.511-19G=
ENST00000360608.9:c.874G= ENSP00000353820.5:p.Asp292=
ENST00000389970.7:c.808G= ENSP00000374620.4:p.Asp270=
ENST00000488442.1:n.1598G=
NM_000106.5:c.874G= NP_000097.3:p.Asp292=
NM_001025161.2:c.721G= NP_001020332.2:p.Asp241=
XM_011529966.1:c.874G= XP_011528268.1:p.Asp292=
XM_011529967.1:c.874G= XP_011528269.1:p.Asp292=
XM_011529968.1:c.874G= XP_011528270.1:p.Asp292=
XM_011529969.1:c.730G= XP_011528271.1:p.Asp244=
XM_011529970.1:c.721G= XP_011528272.1:p.Asp241=
XM_011529971.1:c.730G= XP_011528273.1:p.Asp244=
XM_011529972.1:c.843+221G= XP_011528274.1:n.843+221G=
NM_000106.6:c.874G= MANE Select NP_000097.3:p.Asp292=
NM_001025161.3:c.721G= NP_001020332.2:p.Asp241=