Canonical Allele Identifier: CA2406577823
Gene: CYP2D6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42126628_42126630delinsGAC , CM000684.2:g.42126628_42126630delinsGAC GRCh38
NC_000022.10:g.42522630_42522632delinsGAC , CM000684.1:g.42522630_42522632delinsGAC GRCh37
NC_000022.9:g.40852574_40852576delinsGAC NCBI36
NG_008376.3:g.8362_8364delinsGTC
NG_008376.4:g.9181_9183delinsGTC

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.1236_1238delinsGTC ENSP00000353241.6:n.1236_1238delinsGTC
ENST00000645361.2:c.1438_1440delinsGTC MANE Select ENSP00000496150.1:p.Val480=
ENST00000359033.4:c.1285_1287delinsGTC ENSP00000351927.4:p.Val429=
ENST00000360124.9:c.1056_1058delinsGTC ENSP00000353241.5:n.1056_1058delinsGTC
ENST00000360608.9:c.1438_1440delinsGTC ENSP00000353820.5:p.Val480=
ENST00000389970.7:c.1429_1431delinsGTC ENSP00000374620.4:p.Val477=
ENST00000488442.1:n.2162_2164delinsGTC
NM_000106.5:c.1438_1440delinsGTC NP_000097.3:p.Val480=
NM_001025161.2:c.1285_1287delinsGTC NP_001020332.2:p.Val429=
XM_011529966.1:c.1438_1440delinsGTC XP_011528268.1:p.Val480=
XM_011529967.1:c.1438_1440delinsGTC XP_011528269.1:p.Val480=
XM_011529968.1:c.1438_1440delinsGTC XP_011528270.1:p.Val480=
XM_011529969.1:c.1294_1296delinsGTC XP_011528271.1:p.Val432=
XM_011529970.1:c.1285_1287delinsGTC XP_011528272.1:p.Val429=
XM_011529971.1:c.1294_1296delinsGTC XP_011528273.1:p.Val432=
NM_000106.6:c.1438_1440delinsGTC MANE Select NP_000097.3:p.Val480=
NM_001025161.3:c.1285_1287delinsGTC NP_001020332.2:p.Val429=