Canonical Allele Identifier: CA2577737067
Gene: CYP2D6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42126503_42126504insG , CM000684.2:g.42126503_42126504insG GRCh38
NC_000022.10:g.42522505_42522506insG , CM000684.1:g.42522505_42522506insG GRCh37
NC_000022.9:g.40852449_40852450insG NCBI36
NG_008376.3:g.8488_8489insC
NG_008376.4:g.9307_9308insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000360124.10:c.1362_1363insC ENSP00000353241.6:n.1362_1363insC
ENST00000645361.2:c.*70_*71insC MANE Select ENSP00000496150.1:n.*70_*71insC
ENST00000360124.9:c.1182_1183insC ENSP00000353241.5:n.1182_1183insC
ENST00000360608.9:c.*70_*71insC ENSP00000353820.5:n.*70_*71insC
ENST00000389970.7:c.*70_*71insC ENSP00000374620.4:n.*70_*71insC
NM_000106.5:c.*70_*71insC NP_000097.3:n.*70_*71insC
NM_001025161.2:c.*70_*71insC NP_001020332.2:n.*70_*71insC
XM_011529966.1:c.1452+112_1452+113insC XP_011528268.1:n.1452+112_1452+113insC
XM_011529967.1:c.1452+112_1452+113insC XP_011528269.1:n.1452+112_1452+113insC
XM_011529968.1:c.1452+112_1452+113insC XP_011528270.1:n.1452+112_1452+113insC
XM_011529969.1:c.1308+112_1308+113insC XP_011528271.1:n.1308+112_1308+113insC
XM_011529970.1:c.1299+112_1299+113insC XP_011528272.1:n.1299+112_1299+113insC
XM_011529971.1:c.*70_*71insC XP_011528273.1:n.*70_*71insC
NM_000106.6:c.*70_*71insC MANE Select NP_000097.3:n.*70_*71insC
NM_001025161.3:c.*70_*71insC NP_001020332.2:n.*70_*71insC