Canonical Allele Identifier: CA2336178896
Gene: CYP2A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848461_40848463delinsCCT , CM000681.2:g.40848461_40848463delinsCCT GRCh38
NC_000019.9:g.41354366_41354368delinsCCT , CM000681.1:g.41354366_41354368delinsCCT GRCh37
NC_000019.8:g.46046206_46046208delinsCCT NCBI36
NG_008377.1:g.6985_6987delinsAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.494-84_494-82delinsAGG MANE Select ENSP00000301141.4:n.494-84_494-82delinsAGG
ENST00000301141.9:c.494-84_494-82delinsAGG ENSP00000301141.4:n.494-84_494-82delinsAGG
ENST00000596719.5:n.345-84_345-82delinsAGG
ENST00000600495.1:c.*306-84_*306-82delinsAGG ENSP00000472905.1:n.*306-84_*306-82delinsAGG
ENST00000601627.1:c.120-43530_120-43528delinsCCT
ENST00000610301.1:c.494-84_494-82delinsAGG ENSP00000477899.1:n.494-84_494-82delinsAGG
NM_000762.5:c.494-84_494-82delinsAGG NP_000753.3:n.494-84_494-82delinsAGG
NM_000762.6:c.494-84_494-82delinsAGG MANE Select NP_000753.3:n.494-84_494-82delinsAGG