Canonical Allele Identifier: CA920373717
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1602578815

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128960_42128961insAG , CM000684.2:g.42128960_42128961insAG GRCh38
NC_000022.10:g.42524962_42524963insAG , CM000684.1:g.42524962_42524963insAG GRCh37
NC_000022.9:g.40854906_40854907insAG NCBI36
NG_008376.3:g.6032_6033insTC
NG_008376.4:g.6851_6852insTC

Transcript Alleles

HGVS Amino-acid change
ENST00000645361.2:c.506-16_506-15insTC MANE Select ENSP00000496150.1:n.506-16_506-15insTC
ENST00000359033.4:c.353-16_353-15insTC ENSP00000351927.4:n.353-16_353-15insTC
ENST00000360124.9:n.173-16_173-15insTC ENSP00000353241.5:n.173-16_173-15insTC
ENST00000360608.9:c.506-16_506-15insTC ENSP00000353820.5:n.506-16_506-15insTC
ENST00000389970.7:c.440-16_440-15insTC ENSP00000374620.4:n.440-16_440-15insTC
ENST00000488442.1:n.1230-16_1230-15insTC
NM_000106.5:c.506-16_506-15insTC NP_000097.3:n.506-16_506-15insTC
NM_001025161.2:c.353-16_353-15insTC NP_001020332.2:n.353-16_353-15insTC
XM_011529966.1:c.506-16_506-15insTC XP_011528268.1:n.506-16_506-15insTC
XM_011529967.1:c.506-16_506-15insTC XP_011528269.1:n.506-16_506-15insTC
XM_011529968.1:c.506-16_506-15insTC XP_011528270.1:n.506-16_506-15insTC
XM_011529969.1:c.363-17_363-16insTC XP_011528271.1:n.363-17_363-16insTC
XM_011529970.1:c.353-16_353-15insTC XP_011528272.1:n.353-16_353-15insTC
XM_011529971.1:c.363-17_363-16insTC XP_011528273.1:n.363-17_363-16insTC
XM_011529972.1:c.506-16_506-15insTC XP_011528274.1:n.506-16_506-15insTC
NM_000106.6:c.506-16_506-15insTC MANE Select NP_000097.3:n.506-16_506-15insTC
NM_001025161.3:c.353-16_353-15insTC NP_001020332.2:n.353-16_353-15insTC