Canonical Allele Identifier: CA411774650
Gene: CYP2D6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.42129085del (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42129085del , CM000684.2:g.42129085del GRCh38
NC_000022.10:g.42525087del , CM000684.1:g.42525087del GRCh37
NC_000022.9:g.40855031del NCBI36
NG_008376.3:g.5907del
NG_008376.4:g.6726del

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.353-141del ENSP00000353241.6:n.353-141del
ENST00000645361.2:c.453del MANE Select ENSP00000496150.1:p.Gln151HisfsTer3
ENST00000359033.4:c.353-141del ENSP00000351927.4:n.353-141del
ENST00000360124.9:c.173-141del ENSP00000353241.5:n.173-141del
ENST00000360608.9:c.453del ENSP00000353820.5:p.Gln151HisfsTer3
ENST00000389970.7:c.387del ENSP00000374620.4:p.Gln129HisfsTer3
ENST00000488442.1:n.1177del
NM_000106.5:c.453del NP_000097.3:p.Gln151HisfsTer3
NM_001025161.2:c.353-141del NP_001020332.2:n.353-141del
XM_011529966.1:c.453del XP_011528268.1:p.Gln151HisfsTer3
XM_011529967.1:c.453del XP_011528269.1:p.Gln151HisfsTer3
XM_011529968.1:c.453del XP_011528270.1:p.Gln151HisfsTer3
XM_011529969.1:c.310del XP_011528271.1:p.Val104TrpfsTer?
XM_011529970.1:c.353-141del XP_011528272.1:n.353-141del
XM_011529971.1:c.310del XP_011528273.1:p.Val104TrpfsTer?
XM_011529972.1:c.453del XP_011528274.1:p.Gln151HisfsTer3
NM_000106.6:c.453del MANE Select NP_000097.3:p.Gln151HisfsTer3
NM_001025161.3:c.353-141del NP_001020332.2:n.353-141del