Canonical Allele Identifier: CA639827952
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1370220831

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128245_42128250del , CM000684.2:g.42128245_42128250del GRCh38
NC_000022.10:g.42524247_42524252del , CM000684.1:g.42524247_42524252del GRCh37
NC_000022.9:g.40854191_40854196del NCBI36
NG_008376.3:g.6742_6747del
NG_008376.4:g.7561_7566del

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.614_619del ENSP00000353241.6:p.Thr205_His207delinsAs...
ENST00000645361.2:c.767_772del MANE Select ENSP00000496150.1:p.Thr256_His258delinsAs...
ENST00000359033.4:c.614_619del ENSP00000351927.4:p.Thr205_His207delinsAs...
ENST00000360124.9:c.434_439del ENSP00000353241.5:p.Thr145_His147delinsAs...
ENST00000360608.9:c.767_772del ENSP00000353820.5:p.Thr256_His258delinsAs...
ENST00000389970.7:c.701_706del ENSP00000374620.4:p.Thr234_His236delinsAs...
ENST00000488442.1:n.1491_1496del
NM_000106.5:c.767_772del NP_000097.3:p.Thr256_His258delinsAsn
NM_001025161.2:c.614_619del NP_001020332.2:p.Thr205_His207delinsAsn
XM_011529966.1:c.767_772del XP_011528268.1:p.Thr256_His258delinsAsn
XM_011529967.1:c.767_772del XP_011528269.1:p.Thr256_His258delinsAsn
XM_011529968.1:c.767_772del XP_011528270.1:p.Thr256_His258delinsAsn
XM_011529969.1:c.623_628del XP_011528271.1:p.Thr208_His210delinsAsn
XM_011529970.1:c.614_619del XP_011528272.1:p.Thr205_His207delinsAsn
XM_011529971.1:c.623_628del XP_011528273.1:p.Thr208_His210delinsAsn
XM_011529972.1:c.767_772del XP_011528274.1:p.Thr256_His258delinsAsn
NM_000106.6:c.767_772del MANE Select NP_000097.3:p.Thr256_His258delinsAsn
NM_001025161.3:c.614_619del NP_001020332.2:p.Thr205_His207delinsAsn