Canonical Allele Identifier: CA2819054033
Gene: CYP2D6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42127826_42127827insGGGC , CM000684.2:g.42127826_42127827insGGGC GRCh38
NC_000022.10:g.42523828_42523829insGGGC , CM000684.1:g.42523828_42523829insGGGC GRCh37
NC_000022.9:g.40853772_40853773insGGGC NCBI36
NG_008376.3:g.7165_7166insGCCC
NG_008376.4:g.7984_7985insGCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000360124.10:c.783+15_783+16insGCCC ENSP00000353241.6:n.783+15_783+16insGCCC
ENST00000645361.2:c.985+15_985+16insGCCC MANE Select ENSP00000496150.1:n.985+15_985+16insGCCC
ENST00000359033.4:c.832+15_832+16insGCCC ENSP00000351927.4:n.832+15_832+16insGCCC
ENST00000360124.9:c.603+15_603+16insGCCC ENSP00000353241.5:n.603+15_603+16insGCCC
ENST00000360608.9:c.985+15_985+16insGCCC ENSP00000353820.5:n.985+15_985+16insGCCC
ENST00000389970.7:c.919+15_920-17insGCCC ENSP00000374620.4:n.919+15_920-17insGCCC
ENST00000488442.1:n.1709+15_1709+16insGCCC
NM_000106.5:c.985+15_985+16insGCCC NP_000097.3:n.985+15_985+16insGCCC
NM_001025161.2:c.832+15_832+16insGCCC NP_001020332.2:n.832+15_832+16insGCCC
XM_011529966.1:c.985+15_985+16insGCCC XP_011528268.1:n.985+15_985+16insGCCC
XM_011529967.1:c.985+15_985+16insGCCC XP_011528269.1:n.985+15_985+16insGCCC
XM_011529968.1:c.985+15_985+16insGCCC XP_011528270.1:n.985+15_985+16insGCCC
XM_011529969.1:c.841+15_841+16insGCCC XP_011528271.1:n.841+15_841+16insGCCC
XM_011529970.1:c.832+15_832+16insGCCC XP_011528272.1:n.832+15_832+16insGCCC
XM_011529971.1:c.841+15_841+16insGCCC XP_011528273.1:n.841+15_841+16insGCCC
XM_011529972.1:c.844-193_844-192insGCCC XP_011528274.1:n.844-193_844-192insGCCC
NM_000106.6:c.985+15_985+16insGCCC MANE Select NP_000097.3:n.985+15_985+16insGCCC
NM_001025161.3:c.832+15_832+16insGCCC NP_001020332.2:n.832+15_832+16insGCCC