Canonical Allele Identifier: CA658083275
Gene: CYP2D6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42126548_42126549insA , CM000684.2:g.42126548_42126549insA GRCh38
NC_000022.10:g.42522550_42522551insA , CM000684.1:g.42522550_42522551insA GRCh37
NC_000022.9:g.40852494_40852495insA NCBI36
NG_008376.3:g.8443_8444insT
NG_008376.4:g.9262_9263insT

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.1317_1318insT ENSP00000353241.6:n.1317_1318insT
ENST00000645361.2:c.*25_*26insT MANE Select ENSP00000496150.1:n.*25_*26insT
ENST00000360124.9:c.1137_1138insT ENSP00000353241.5:n.1137_1138insT
ENST00000360608.9:c.*25_*26insT ENSP00000353820.5:n.*25_*26insT
ENST00000389970.7:c.*25_*26insT ENSP00000374620.4:n.*25_*26insT
ENST00000488442.1:n.2243_2244insT
NM_000106.5:c.*25_*26insT NP_000097.3:n.*25_*26insT
NM_001025161.2:c.*25_*26insT NP_001020332.2:n.*25_*26insT
XM_011529966.1:c.1452+67_1452+68insT XP_011528268.1:n.1452+67_1452+68insT
XM_011529967.1:c.1452+67_1452+68insT XP_011528269.1:n.1452+67_1452+68insT
XM_011529968.1:c.1452+67_1452+68insT XP_011528270.1:n.1452+67_1452+68insT
XM_011529969.1:c.1308+67_1308+68insT XP_011528271.1:n.1308+67_1308+68insT
XM_011529970.1:c.1299+67_1299+68insT XP_011528272.1:n.1299+67_1299+68insT
XM_011529971.1:c.*25_*26insT XP_011528273.1:n.*25_*26insT
NM_000106.6:c.*25_*26insT MANE Select NP_000097.3:n.*25_*26insT
NM_001025161.3:c.*25_*26insT NP_001020332.2:n.*25_*26insT