Canonical Allele Identifier: CA2657031401
Gene: CYP2D6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42130569_42130570insTGGGGC , CM000684.2:g.42130569_42130570insTGGGGC GRCh38
NC_000022.10:g.42526571_42526572insTGGGGC , CM000684.1:g.42526571_42526572insTGGGGC GRCh37
NC_000022.9:g.40856515_40856516insTGGGGC NCBI36
NG_008376.3:g.4422_4423insGCCCCA
NG_008376.4:g.5241_5242insGCCCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000360124.10:c.180+42_180+43insGCCCCA ENSP00000353241.6:n.180+42_180+43insGCCCCA
ENST00000645361.2:c.180+42_180+43insGCCCCA MANE Select ENSP00000496150.1:n.180+42_180+43insGCCCCA
ENST00000359033.4:c.180+42_180+43insGCCCCA ENSP00000351927.4:n.180+42_180+43insGCCCCA
ENST00000360608.9:c.180+42_180+43insGCCCCA ENSP00000353820.5:n.180+42_180+43insGCCCCA
ENST00000389970.7:c.114+42_114+43insGCCCCA ENSP00000374620.4:n.114+42_114+43insGCCCCA
ENST00000488442.1:n.244_245insGCCCCA
NM_000106.5:c.180+42_180+43insGCCCCA NP_000097.3:n.180+42_180+43insGCCCCA
NM_001025161.2:c.180+42_180+43insGCCCCA NP_001020332.2:n.180+42_180+43insGCCCCA
XM_011529966.1:c.180+42_180+43insGCCCCA XP_011528268.1:n.180+42_180+43insGCCCCA
XM_011529967.1:c.180+42_180+43insGCCCCA XP_011528269.1:n.180+42_180+43insGCCCCA
XM_011529968.1:c.180+42_180+43insGCCCCA XP_011528270.1:n.180+42_180+43insGCCCCA
XM_011529969.1:c.38-661_38-660insGCCCCA XP_011528271.1:n.38-661_38-660insGCCCCA
XM_011529970.1:c.180+42_180+43insGCCCCA XP_011528272.1:n.180+42_180+43insGCCCCA
XM_011529971.1:c.38-661_38-660insGCCCCA XP_011528273.1:n.38-661_38-660insGCCCCA
XM_011529972.1:c.180+42_180+43insGCCCCA XP_011528274.1:n.180+42_180+43insGCCCCA
XR_430455.2:n.209_210insTGGGGC
NM_000106.6:c.180+42_180+43insGCCCCA MANE Select NP_000097.3:n.180+42_180+43insGCCCCA
XR_002958749.1:n.156_157insTGGGGC
NM_001025161.3:c.180+42_180+43insGCCCCA NP_001020332.2:n.180+42_180+43insGCCCCA