Canonical Allele Identifier: CA411772354
Gene: CYP2D6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42127847A>G , CM000684.2:g.42127847A>G GRCh38
NC_000022.10:g.42523849A>G , CM000684.1:g.42523849A>G GRCh37
NC_000022.9:g.40853793A>G NCBI36
NG_008376.3:g.7145T>C
NG_008376.4:g.7964T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.778T>C ENSP00000353241.6:n.778T>C
ENST00000645361.2:c.980T>C MANE Select ENSP00000496150.1:p.Val327Ala
ENST00000359033.4:c.827T>C ENSP00000351927.4:p.Val276Ala
ENST00000360124.9:c.598T>C ENSP00000353241.5:n.598T>C
ENST00000360608.9:c.980T>C ENSP00000353820.5:p.Val327Ala
ENST00000389970.7:c.914T>C ENSP00000374620.4:p.Val305Ala
ENST00000488442.1:n.1704T>C
NM_000106.5:c.980T>C NP_000097.3:p.Val327Ala
NM_001025161.2:c.827T>C NP_001020332.2:p.Val276Ala
XM_011529966.1:c.980T>C XP_011528268.1:p.Val327Ala
XM_011529967.1:c.980T>C XP_011528269.1:p.Val327Ala
XM_011529968.1:c.980T>C XP_011528270.1:p.Val327Ala
XM_011529969.1:c.836T>C XP_011528271.1:p.Val279Ala
XM_011529970.1:c.827T>C XP_011528272.1:p.Val276Ala
XM_011529971.1:c.836T>C XP_011528273.1:p.Val279Ala
XM_011529972.1:c.844-213T>C XP_011528274.1:n.844-213T>C
NM_000106.6:c.980T>C MANE Select NP_000097.3:p.Val327Ala
NM_001025161.3:c.827T>C NP_001020332.2:p.Val276Ala