Canonical Allele Identifier: CA411773354
Gene: CYP2D6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128258C>A , CM000684.2:g.42128258C>A GRCh38
NC_000022.10:g.42524260C>A , CM000684.1:g.42524260C>A GRCh37
NC_000022.9:g.40854204C>A NCBI36
NG_008376.3:g.6734G>T
NG_008376.4:g.7553G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360124.10:c.606G>T ENSP00000353241.6:p.Glu202Asp
ENST00000645361.2:c.759G>T MANE Select ENSP00000496150.1:p.Glu253Asp
ENST00000359033.4:c.606G>T ENSP00000351927.4:p.Glu202Asp
ENST00000360124.9:c.426G>T ENSP00000353241.5:p.Glu142Asp
ENST00000360608.9:c.759G>T ENSP00000353820.5:p.Glu253Asp
ENST00000389970.7:c.693G>T ENSP00000374620.4:p.Glu231Asp
ENST00000488442.1:n.1483G>T
NM_000106.5:c.759G>T NP_000097.3:p.Glu253Asp
NM_001025161.2:c.606G>T NP_001020332.2:p.Glu202Asp
XM_011529966.1:c.759G>T XP_011528268.1:p.Glu253Asp
XM_011529967.1:c.759G>T XP_011528269.1:p.Glu253Asp
XM_011529968.1:c.759G>T XP_011528270.1:p.Glu253Asp
XM_011529969.1:c.615G>T XP_011528271.1:p.Glu205Asp
XM_011529970.1:c.606G>T XP_011528272.1:p.Glu202Asp
XM_011529971.1:c.615G>T XP_011528273.1:p.Glu205Asp
XM_011529972.1:c.759G>T XP_011528274.1:p.Glu253Asp
NM_000106.6:c.759G>T MANE Select NP_000097.3:p.Glu253Asp
NM_001025161.3:c.606G>T NP_001020332.2:p.Glu202Asp