Canonical Allele Identifier: CA2406580028
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1931644916

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42129429_42129443del , CM000684.2:g.42129429_42129443del GRCh38
NC_000022.10:g.42525431_42525445del , CM000684.1:g.42525431_42525445del GRCh37
NC_000022.9:g.40855375_40855389del NCBI36
NG_008376.3:g.5549_5563del
NG_008376.4:g.6368_6382del

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.352+295_352+309del ENSP00000353241.6:n.352+295_352+309del
ENST00000645361.2:c.353-258_353-244del MANE Select ENSP00000496150.1:n.353-258_353-244del
ENST00000359033.4:c.352+295_352+309del ENSP00000351927.4:n.352+295_352+309del
ENST00000360124.9:c.172+295_172+309del ENSP00000353241.5:n.172+295_172+309del
ENST00000360608.9:c.353-258_353-244del ENSP00000353820.5:n.353-258_353-244del
ENST00000389970.7:c.287-258_287-244del ENSP00000374620.4:n.287-258_287-244del
ENST00000488442.1:n.1077-258_1077-244del
NM_000106.5:c.353-258_353-244del NP_000097.3:n.353-258_353-244del
NM_001025161.2:c.352+295_352+309del NP_001020332.2:n.352+295_352+309del
XM_011529966.1:c.353-258_353-244del XP_011528268.1:n.353-258_353-244del
XM_011529967.1:c.353-258_353-244del XP_011528269.1:n.353-258_353-244del
XM_011529968.1:c.353-258_353-244del XP_011528270.1:n.353-258_353-244del
XM_011529969.1:c.210-258_210-244del XP_011528271.1:n.210-258_210-244del
XM_011529970.1:c.352+295_352+309del XP_011528272.1:n.352+295_352+309del
XM_011529971.1:c.210-258_210-244del XP_011528273.1:n.210-258_210-244del
XM_011529972.1:c.353-258_353-244del XP_011528274.1:n.353-258_353-244del
NM_000106.6:c.353-258_353-244del MANE Select NP_000097.3:n.353-258_353-244del
NM_001025161.3:c.352+295_352+309del NP_001020332.2:n.352+295_352+309del