Canonical Allele Identifier: CA2406577817
Gene: CYP2D6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42126622A= , CM000684.2:g.42126622A= GRCh38
NC_000022.10:g.42522624A= , CM000684.1:g.42522624A= GRCh37
NC_000022.9:g.40852568A= NCBI36
NG_008376.3:g.8370T=
NG_008376.4:g.9189T=

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.1244T= ENSP00000353241.6:n.1244T=
ENST00000645361.2:c.1446T= MANE Select ENSP00000496150.1:p.Ala482=
ENST00000359033.4:c.1293T= ENSP00000351927.4:p.Ala431=
ENST00000360124.9:c.1064T= ENSP00000353241.5:n.1064T=
ENST00000360608.9:c.1446T= ENSP00000353820.5:p.Ala482=
ENST00000389970.7:c.1437T= ENSP00000374620.4:p.Ala479=
ENST00000488442.1:n.2170T=
NM_000106.5:c.1446T= NP_000097.3:p.Ala482=
NM_001025161.2:c.1293T= NP_001020332.2:p.Ala431=
XM_011529966.1:c.1446T= XP_011528268.1:p.Ala482=
XM_011529967.1:c.1446T= XP_011528269.1:p.Ala482=
XM_011529968.1:c.1446T= XP_011528270.1:p.Ala482=
XM_011529969.1:c.1302T= XP_011528271.1:p.Ala434=
XM_011529970.1:c.1293T= XP_011528272.1:p.Ala431=
XM_011529971.1:c.1302T= XP_011528273.1:p.Ala434=
NM_000106.6:c.1446T= MANE Select NP_000097.3:p.Ala482=
NM_001025161.3:c.1293T= NP_001020332.2:p.Ala431=