Canonical Allele Identifier: CA2657031111
Gene: CYP2D6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42130376dup , CM000684.2:g.42130376dup GRCh38
NC_000022.10:g.42526378dup , CM000684.1:g.42526378dup GRCh37
NC_000022.9:g.40856322dup NCBI36
NG_008376.3:g.4616dup
NG_008376.4:g.5435dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000360124.10:c.180+236dup ENSP00000353241.6:n.180+236dup
ENST00000645361.2:c.180+236dup MANE Select ENSP00000496150.1:n.180+236dup
ENST00000359033.4:c.180+236dup ENSP00000351927.4:n.180+236dup
ENST00000360608.9:c.180+236dup ENSP00000353820.5:n.180+236dup
ENST00000389970.7:c.114+236dup ENSP00000374620.4:n.114+236dup
ENST00000488442.1:n.438dup
NM_000106.5:c.180+236dup NP_000097.3:n.180+236dup
NM_001025161.2:c.180+236dup NP_001020332.2:n.180+236dup
XM_011529966.1:c.180+236dup XP_011528268.1:n.180+236dup
XM_011529967.1:c.180+236dup XP_011528269.1:n.180+236dup
XM_011529968.1:c.180+236dup XP_011528270.1:n.180+236dup
XM_011529969.1:c.38-467dup XP_011528271.1:n.38-467dup
XM_011529970.1:c.180+236dup XP_011528272.1:n.180+236dup
XM_011529971.1:c.38-467dup XP_011528273.1:n.38-467dup
XM_011529972.1:c.180+236dup XP_011528274.1:n.180+236dup
XR_430455.2:n.206+153dup
NM_000106.6:c.180+236dup MANE Select NP_000097.3:n.180+236dup
XR_002958749.1:n.153+153dup
NM_001025161.3:c.180+236dup NP_001020332.2:n.180+236dup