Canonical Allele Identifier: CA639827872
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs1287881057

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42126509_42126511del , CM000684.2:g.42126509_42126511del GRCh38
NC_000022.10:g.42522511_42522513del , CM000684.1:g.42522511_42522513del GRCh37
NC_000022.9:g.40852455_40852457del NCBI36
NG_008376.3:g.8483_8485del
NG_008376.4:g.9302_9304del

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.1357_1359del ENSP00000353241.6:n.1357_1359del
ENST00000645361.2:c.*65_*67del MANE Select ENSP00000496150.1:n.*65_*67del
ENST00000360124.9:c.1177_1179del ENSP00000353241.5:n.1177_1179del
ENST00000360608.9:c.*65_*67del ENSP00000353820.5:n.*65_*67del
ENST00000389970.7:c.*65_*67del ENSP00000374620.4:n.*65_*67del
NM_000106.5:c.*65_*67del NP_000097.3:n.*65_*67del
NM_001025161.2:c.*65_*67del NP_001020332.2:n.*65_*67del
XM_011529966.1:c.1452+107_1452+109del XP_011528268.1:n.1452+107_1452+109del
XM_011529967.1:c.1452+107_1452+109del XP_011528269.1:n.1452+107_1452+109del
XM_011529968.1:c.1452+107_1452+109del XP_011528270.1:n.1452+107_1452+109del
XM_011529969.1:c.1308+107_1308+109del XP_011528271.1:n.1308+107_1308+109del
XM_011529970.1:c.1299+107_1299+109del XP_011528272.1:n.1299+107_1299+109del
XM_011529971.1:c.*65_*67del XP_011528273.1:n.*65_*67del
NM_000106.6:c.*65_*67del MANE Select NP_000097.3:n.*65_*67del
NM_001025161.3:c.*65_*67del NP_001020332.2:n.*65_*67del