Canonical Allele Identifier: CA2841230362
Gene: CYP2D6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42130563_42130564dup , CM000684.2:g.42130563_42130564dup GRCh38
NC_000022.10:g.42526565_42526566dup , CM000684.1:g.42526565_42526566dup GRCh37
NC_000022.9:g.40856509_40856510dup NCBI36
NG_008376.3:g.4428_4429dup
NG_008376.4:g.5247_5248dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000360124.10:c.180+48_180+49dup ENSP00000353241.6:n.180+48_180+49dup
ENST00000645361.2:c.180+48_180+49dup MANE Select ENSP00000496150.1:n.180+48_180+49dup
ENST00000359033.4:c.180+48_180+49dup ENSP00000351927.4:n.180+48_180+49dup
ENST00000360608.9:c.180+48_180+49dup ENSP00000353820.5:n.180+48_180+49dup
ENST00000389970.7:c.114+48_114+49dup ENSP00000374620.4:n.114+48_114+49dup
ENST00000488442.1:n.250_251dup
NM_000106.5:c.180+48_180+49dup NP_000097.3:n.180+48_180+49dup
NM_001025161.2:c.180+48_180+49dup NP_001020332.2:n.180+48_180+49dup
XM_011529966.1:c.180+48_180+49dup XP_011528268.1:n.180+48_180+49dup
XM_011529967.1:c.180+48_180+49dup XP_011528269.1:n.180+48_180+49dup
XM_011529968.1:c.180+48_180+49dup XP_011528270.1:n.180+48_180+49dup
XM_011529969.1:c.38-655_38-654dup XP_011528271.1:n.38-655_38-654dup
XM_011529970.1:c.180+48_180+49dup XP_011528272.1:n.180+48_180+49dup
XM_011529971.1:c.38-655_38-654dup XP_011528273.1:n.38-655_38-654dup
XM_011529972.1:c.180+48_180+49dup XP_011528274.1:n.180+48_180+49dup
XR_430455.2:n.207-4_207-3dup
NM_000106.6:c.180+48_180+49dup MANE Select NP_000097.3:n.180+48_180+49dup
XR_002958749.1:n.154-4_154-3dup
NM_001025161.3:c.180+48_180+49dup NP_001020332.2:n.180+48_180+49dup