Canonical Allele Identifier: CA2657031220
Gene: CYP2D6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42127795_42127801del , CM000684.2:g.42127795_42127801del GRCh38
NC_000022.10:g.42523797_42523803del , CM000684.1:g.42523797_42523803del GRCh37
NC_000022.9:g.40853741_40853747del NCBI36
NG_008376.3:g.7194_7200del
NG_008376.4:g.8013_8019del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360124.10:c.783+44_783+50del ENSP00000353241.6:n.783+44_783+50del
ENST00000645361.2:c.985+44_985+50del MANE Select ENSP00000496150.1:n.985+44_985+50del
ENST00000359033.4:c.832+44_832+50del ENSP00000351927.4:n.832+44_832+50del
ENST00000360124.9:c.603+44_603+50del ENSP00000353241.5:n.603+44_603+50del
ENST00000360608.9:c.985+44_985+50del ENSP00000353820.5:n.985+44_985+50del
ENST00000389970.7:c.931_937del ENSP00000374620.4:p.Val311ArgfsTer23
ENST00000488442.1:n.1709+44_1709+50del
NM_000106.5:c.985+44_985+50del NP_000097.3:n.985+44_985+50del
NM_001025161.2:c.832+44_832+50del NP_001020332.2:n.832+44_832+50del
XM_011529966.1:c.985+44_985+50del XP_011528268.1:n.985+44_985+50del
XM_011529967.1:c.985+44_985+50del XP_011528269.1:n.985+44_985+50del
XM_011529968.1:c.985+44_985+50del XP_011528270.1:n.985+44_985+50del
XM_011529969.1:c.841+44_841+50del XP_011528271.1:n.841+44_841+50del
XM_011529970.1:c.832+44_832+50del XP_011528272.1:n.832+44_832+50del
XM_011529971.1:c.841+44_841+50del XP_011528273.1:n.841+44_841+50del
XM_011529972.1:c.844-164_844-158del XP_011528274.1:n.844-164_844-158del
NM_000106.6:c.985+44_985+50del MANE Select NP_000097.3:n.985+44_985+50del
NM_001025161.3:c.832+44_832+50del NP_001020332.2:n.832+44_832+50del