Canonical Allele Identifier: CA2657031591
Gene: CYP2D6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128159_42128168del , CM000684.2:g.42128159_42128168del GRCh38
NC_000022.10:g.42524161_42524170del , CM000684.1:g.42524161_42524170del GRCh37
NC_000022.9:g.40854105_40854114del NCBI36
NG_008376.3:g.6825_6834del
NG_008376.4:g.7644_7653del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360124.10:c.690+7_690+16del ENSP00000353241.6:n.690+7_690+16del
ENST00000645361.2:c.843+7_843+16del MANE Select ENSP00000496150.1:n.843+7_843+16del
ENST00000359033.4:c.690+7_690+16del ENSP00000351927.4:n.690+7_690+16del
ENST00000360124.9:c.510+7_510+16del ENSP00000353241.5:n.510+7_510+16del
ENST00000360608.9:c.843+7_843+16del ENSP00000353820.5:n.843+7_843+16del
ENST00000389970.7:c.777+7_777+16del ENSP00000374620.4:n.777+7_777+16del
ENST00000488442.1:n.1567+7_1567+16del
NM_000106.5:c.843+7_843+16del NP_000097.3:n.843+7_843+16del
NM_001025161.2:c.690+7_690+16del NP_001020332.2:n.690+7_690+16del
XM_011529966.1:c.843+7_843+16del XP_011528268.1:n.843+7_843+16del
XM_011529967.1:c.843+7_843+16del XP_011528269.1:n.843+7_843+16del
XM_011529968.1:c.843+7_843+16del XP_011528270.1:n.843+7_843+16del
XM_011529969.1:c.699+7_699+16del XP_011528271.1:n.699+7_699+16del
XM_011529970.1:c.690+7_690+16del XP_011528272.1:n.690+7_690+16del
XM_011529971.1:c.699+7_699+16del XP_011528273.1:n.699+7_699+16del
XM_011529972.1:c.843+7_843+16del XP_011528274.1:n.843+7_843+16del
NM_000106.6:c.843+7_843+16del MANE Select NP_000097.3:n.843+7_843+16del
NM_001025161.3:c.690+7_690+16del NP_001020332.2:n.690+7_690+16del