Canonical Allele Identifier: CA2336178639
Gene: CYP2A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848027_40848030delinsGTGT , CM000681.2:g.40848027_40848030delinsGTGT GRCh38
NC_000019.9:g.41353932_41353935delinsGTGT , CM000681.1:g.41353932_41353935delinsGTGT GRCh37
NC_000019.8:g.46045772_46045775delinsGTGT NCBI36
NG_008377.1:g.7418_7421delinsACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.654+189_654+192delinsACAC MANE Select ENSP00000301141.4:n.654+189_654+192delinsACAC
ENST00000301141.9:c.654+189_654+192delinsACAC ENSP00000301141.4:n.654+189_654+192delinsACAC
ENST00000596719.5:n.505+189_505+192delinsACAC
ENST00000600495.1:c.*466+189_*466+192delinsACAC ENSP00000472905.1:n.*466+189_*466+192delinsACAC
ENST00000601627.1:c.120-43964_120-43961delinsGTGT
ENST00000610301.1:c.654+189_654+192delinsACAC ENSP00000477899.1:n.654+189_654+192delinsACAC
NM_000762.5:c.654+189_654+192delinsACAC NP_000753.3:n.654+189_654+192delinsACAC
NM_000762.6:c.654+189_654+192delinsACAC MANE Select NP_000753.3:n.654+189_654+192delinsACAC