Canonical Allele Identifier: CA2819054035
Gene: CYP2D6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128007_42128008insA , CM000684.2:g.42128007_42128008insA GRCh38
NC_000022.10:g.42524009_42524010insA , CM000684.1:g.42524009_42524010insA GRCh37
NC_000022.9:g.40853953_40853954insA NCBI36
NG_008376.3:g.6984_6985insT
NG_008376.4:g.7803_7804insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000360124.10:c.691-74_691-73insT ENSP00000353241.6:n.691-74_691-73insT
ENST00000645361.2:c.844-25_844-24insT MANE Select ENSP00000496150.1:n.844-25_844-24insT
ENST00000359033.4:c.691-25_691-24insT ENSP00000351927.4:n.691-25_691-24insT
ENST00000360124.9:c.511-74_511-73insT ENSP00000353241.5:n.511-74_511-73insT
ENST00000360608.9:c.844-25_844-24insT ENSP00000353820.5:n.844-25_844-24insT
ENST00000389970.7:c.778-25_778-24insT ENSP00000374620.4:n.778-25_778-24insT
ENST00000488442.1:n.1568-25_1568-24insT
NM_000106.5:c.844-25_844-24insT NP_000097.3:n.844-25_844-24insT
NM_001025161.2:c.691-25_691-24insT NP_001020332.2:n.691-25_691-24insT
XM_011529966.1:c.844-25_844-24insT XP_011528268.1:n.844-25_844-24insT
XM_011529967.1:c.844-25_844-24insT XP_011528269.1:n.844-25_844-24insT
XM_011529968.1:c.844-25_844-24insT XP_011528270.1:n.844-25_844-24insT
XM_011529969.1:c.700-25_700-24insT XP_011528271.1:n.700-25_700-24insT
XM_011529970.1:c.691-25_691-24insT XP_011528272.1:n.691-25_691-24insT
XM_011529971.1:c.700-25_700-24insT XP_011528273.1:n.700-25_700-24insT
XM_011529972.1:c.843+166_843+167insT XP_011528274.1:n.843+166_843+167insT
NM_000106.6:c.844-25_844-24insT MANE Select NP_000097.3:n.844-25_844-24insT
NM_001025161.3:c.691-25_691-24insT NP_001020332.2:n.691-25_691-24insT