Canonical Allele Identifier: CA2406579489
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1931451858

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128810del , CM000684.2:g.42128810del GRCh38
NC_000022.10:g.42524812del , CM000684.1:g.42524812del GRCh37
NC_000022.9:g.40854756del NCBI36
NG_008376.3:g.6183del
NG_008376.4:g.7002del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360124.10:c.488del ENSP00000353241.6:p.Lys163ArgfsTer11
ENST00000645361.2:c.641del MANE Select ENSP00000496150.1:p.Lys214ArgfsTer11
ENST00000359033.4:c.488del ENSP00000351927.4:p.Lys163ArgfsTer11
ENST00000360124.9:c.308del ENSP00000353241.5:p.Lys103ArgfsTer11
ENST00000360608.9:c.641del ENSP00000353820.5:p.Lys214ArgfsTer11
ENST00000389970.7:c.575del ENSP00000374620.4:p.Lys192ArgfsTer11
ENST00000488442.1:n.1365del
NM_000106.5:c.641del NP_000097.3:p.Lys214ArgfsTer11
NM_001025161.2:c.488del NP_001020332.2:p.Lys163ArgfsTer11
XM_011529966.1:c.641del XP_011528268.1:p.Lys214ArgfsTer11
XM_011529967.1:c.641del XP_011528269.1:p.Lys214ArgfsTer11
XM_011529968.1:c.641del XP_011528270.1:p.Lys214ArgfsTer11
XM_011529969.1:c.497del XP_011528271.1:p.Lys166ArgfsTer11
XM_011529970.1:c.488del XP_011528272.1:p.Lys163ArgfsTer11
XM_011529971.1:c.497del XP_011528273.1:p.Lys166ArgfsTer11
XM_011529972.1:c.641del XP_011528274.1:p.Lys214ArgfsTer11
NM_000106.6:c.641del MANE Select NP_000097.3:p.Lys214ArgfsTer11
NM_001025161.3:c.488del NP_001020332.2:p.Lys163ArgfsTer11