Canonical Allele Identifier: CA411772339
Gene: CYP2D6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42127844T>G , CM000684.2:g.42127844T>G GRCh38
NC_000022.10:g.42523846T>G , CM000684.1:g.42523846T>G GRCh37
NC_000022.9:g.40853790T>G NCBI36
NG_008376.3:g.7148A>C
NG_008376.4:g.7967A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.781A>C ENSP00000353241.6:n.781A>C
ENST00000645361.2:c.983A>C MANE Select ENSP00000496150.1:p.Gln328Pro
ENST00000359033.4:c.830A>C ENSP00000351927.4:p.Gln277Pro
ENST00000360124.9:c.601A>C ENSP00000353241.5:n.601A>C
ENST00000360608.9:c.983A>C ENSP00000353820.5:p.Gln328Pro
ENST00000389970.7:c.917A>C ENSP00000374620.4:p.Gln306Pro
ENST00000488442.1:n.1707A>C
NM_000106.5:c.983A>C NP_000097.3:p.Gln328Pro
NM_001025161.2:c.830A>C NP_001020332.2:p.Gln277Pro
XM_011529966.1:c.983A>C XP_011528268.1:p.Gln328Pro
XM_011529967.1:c.983A>C XP_011528269.1:p.Gln328Pro
XM_011529968.1:c.983A>C XP_011528270.1:p.Gln328Pro
XM_011529969.1:c.839A>C XP_011528271.1:p.Gln280Pro
XM_011529970.1:c.830A>C XP_011528272.1:p.Gln277Pro
XM_011529971.1:c.839A>C XP_011528273.1:p.Gln280Pro
XM_011529972.1:c.844-210A>C XP_011528274.1:n.844-210A>C
NM_000106.6:c.983A>C MANE Select NP_000097.3:p.Gln328Pro
NM_001025161.3:c.830A>C NP_001020332.2:p.Gln277Pro