Canonical Allele Identifier: CA2406581017
Gene: CYP2D6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42130598_42130601delinsACCT , CM000684.2:g.42130598_42130601delinsACCT GRCh38
NC_000022.10:g.42526600_42526603delinsACCT , CM000684.1:g.42526600_42526603delinsACCT GRCh37
NC_000022.9:g.40856544_40856547delinsACCT NCBI36
NG_008376.3:g.4391_4394delinsAGGT
NG_008376.4:g.5210_5213delinsAGGT

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.180+11_180+14delinsAGGT ENSP00000353241.6:n.180+11_180+14delinsAG...
ENST00000645361.2:c.180+11_180+14delinsAGGT MANE Select ENSP00000496150.1:n.180+11_180+14delinsAG...
ENST00000359033.4:c.180+11_180+14delinsAGGT ENSP00000351927.4:n.180+11_180+14delinsAG...
ENST00000360608.9:c.180+11_180+14delinsAGGT ENSP00000353820.5:n.180+11_180+14delinsAG...
ENST00000389970.7:c.114+11_114+14delinsAGGT ENSP00000374620.4:n.114+11_114+14delinsAG...
ENST00000488442.1:n.213_216delinsAGGT
NM_000106.5:c.180+11_180+14delinsAGGT NP_000097.3:n.180+11_180+14delinsAGGT
NM_001025161.2:c.180+11_180+14delinsAGGT NP_001020332.2:n.180+11_180+14delinsAGGT
XM_011529966.1:c.180+11_180+14delinsAGGT XP_011528268.1:n.180+11_180+14delinsAGGT
XM_011529967.1:c.180+11_180+14delinsAGGT XP_011528269.1:n.180+11_180+14delinsAGGT
XM_011529968.1:c.180+11_180+14delinsAGGT XP_011528270.1:n.180+11_180+14delinsAGGT
XM_011529969.1:c.38-692_38-689delinsAGGT XP_011528271.1:n.38-692_38-689delinsAGGT
XM_011529970.1:c.180+11_180+14delinsAGGT XP_011528272.1:n.180+11_180+14delinsAGGT
XM_011529971.1:c.38-692_38-689delinsAGGT XP_011528273.1:n.38-692_38-689delinsAGGT
XM_011529972.1:c.180+11_180+14delinsAGGT XP_011528274.1:n.180+11_180+14delinsAGGT
XR_430455.2:n.238_241delinsACCT
NM_000106.6:c.180+11_180+14delinsAGGT MANE Select NP_000097.3:n.180+11_180+14delinsAGGT
XR_002958749.1:n.185_188delinsACCT
NM_001025161.3:c.180+11_180+14delinsAGGT NP_001020332.2:n.180+11_180+14delinsAGGT