Canonical Allele Identifier: CA2406579055
Gene: CYP2D6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128262_42128267delinsTCCAGC , CM000684.2:g.42128262_42128267delinsTCCAGC GRCh38
NC_000022.10:g.42524264_42524269delinsTCCAGC , CM000684.1:g.42524264_42524269delinsTCCAGC GRCh37
NC_000022.9:g.40854208_40854213delinsTCCAGC NCBI36
NG_008376.3:g.6725_6730delinsGCTGGA
NG_008376.4:g.7544_7549delinsGCTGGA

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.597_602delinsGCTGGA ENSP00000353241.6:p.Gln199=
ENST00000645361.2:c.750_755delinsGCTGGA MANE Select ENSP00000496150.1:p.Gln250=
ENST00000359033.4:c.597_602delinsGCTGGA ENSP00000351927.4:p.Gln199=
ENST00000360124.9:c.417_422delinsGCTGGA ENSP00000353241.5:p.Gln139=
ENST00000360608.9:c.750_755delinsGCTGGA ENSP00000353820.5:p.Gln250=
ENST00000389970.7:c.684_689delinsGCTGGA ENSP00000374620.4:p.Gln228=
ENST00000488442.1:n.1474_1479delinsGCTGGA
NM_000106.5:c.750_755delinsGCTGGA NP_000097.3:p.Gln250=
NM_001025161.2:c.597_602delinsGCTGGA NP_001020332.2:p.Gln199=
XM_011529966.1:c.750_755delinsGCTGGA XP_011528268.1:p.Gln250=
XM_011529967.1:c.750_755delinsGCTGGA XP_011528269.1:p.Gln250=
XM_011529968.1:c.750_755delinsGCTGGA XP_011528270.1:p.Gln250=
XM_011529969.1:c.606_611delinsGCTGGA XP_011528271.1:p.Gln202=
XM_011529970.1:c.597_602delinsGCTGGA XP_011528272.1:p.Gln199=
XM_011529971.1:c.606_611delinsGCTGGA XP_011528273.1:p.Gln202=
XM_011529972.1:c.750_755delinsGCTGGA XP_011528274.1:p.Gln250=
NM_000106.6:c.750_755delinsGCTGGA MANE Select NP_000097.3:p.Gln250=
NM_001025161.3:c.597_602delinsGCTGGA NP_001020332.2:p.Gln199=