Canonical Allele Identifier: CA2657035902
Gene: CYP2D6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42129219_42129226del , CM000684.2:g.42129219_42129226del GRCh38
NC_000022.10:g.42525221_42525228del , CM000684.1:g.42525221_42525228del GRCh37
NC_000022.9:g.40855165_40855172del NCBI36
NG_008376.3:g.5769_5776del
NG_008376.4:g.6588_6595del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360124.10:c.353-279_353-272del ENSP00000353241.6:n.353-279_353-272del
ENST00000645361.2:c.353-38_353-31del MANE Select ENSP00000496150.1:n.353-38_353-31del
ENST00000359033.4:c.353-279_353-272del ENSP00000351927.4:n.353-279_353-272del
ENST00000360124.9:c.173-279_173-272del ENSP00000353241.5:n.173-279_173-272del
ENST00000360608.9:c.353-38_353-31del ENSP00000353820.5:n.353-38_353-31del
ENST00000389970.7:c.287-38_287-31del ENSP00000374620.4:n.287-38_287-31del
ENST00000488442.1:n.1077-38_1077-31del
NM_000106.5:c.353-38_353-31del NP_000097.3:n.353-38_353-31del
NM_001025161.2:c.353-279_353-272del NP_001020332.2:n.353-279_353-272del
XM_011529966.1:c.353-38_353-31del XP_011528268.1:n.353-38_353-31del
XM_011529967.1:c.353-38_353-31del XP_011528269.1:n.353-38_353-31del
XM_011529968.1:c.353-38_353-31del XP_011528270.1:n.353-38_353-31del
XM_011529969.1:c.210-38_210-31del XP_011528271.1:n.210-38_210-31del
XM_011529970.1:c.353-279_353-272del XP_011528272.1:n.353-279_353-272del
XM_011529971.1:c.210-38_210-31del XP_011528273.1:n.210-38_210-31del
XM_011529972.1:c.353-38_353-31del XP_011528274.1:n.353-38_353-31del
NM_000106.6:c.353-38_353-31del MANE Select NP_000097.3:n.353-38_353-31del
NM_001025161.3:c.353-279_353-272del NP_001020332.2:n.353-279_353-272del