Canonical Allele Identifier: CA2336178685
Gene: CYP2A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848104_40848105delinsAT , CM000681.2:g.40848104_40848105delinsAT GRCh38
NC_000019.9:g.41354009_41354010delinsAT , CM000681.1:g.41354009_41354010delinsAT GRCh37
NC_000019.8:g.46045849_46045850delinsAT NCBI36
NG_008377.1:g.7343_7344delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.654+114_654+115delinsAT MANE Select ENSP00000301141.4:n.654+114_654+115delinsAT
ENST00000301141.9:c.654+114_654+115delinsAT ENSP00000301141.4:n.654+114_654+115delinsAT
ENST00000596719.5:n.505+114_505+115delinsAT
ENST00000600495.1:c.*466+114_*466+115delinsAT ENSP00000472905.1:n.*466+114_*466+115delinsAT
ENST00000601627.1:c.120-43887_120-43886delinsAT
ENST00000610301.1:c.654+114_654+115delinsAT ENSP00000477899.1:n.654+114_654+115delinsAT
NM_000762.5:c.654+114_654+115delinsAT NP_000753.3:n.654+114_654+115delinsAT
NM_000762.6:c.654+114_654+115delinsAT MANE Select NP_000753.3:n.654+114_654+115delinsAT