Canonical Allele Identifier: CA2336178626
Gene: CYP2A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40847992_40847994delinsGCT , CM000681.2:g.40847992_40847994delinsGCT GRCh38
NC_000019.9:g.41353897_41353899delinsGCT , CM000681.1:g.41353897_41353899delinsGCT GRCh37
NC_000019.8:g.46045737_46045739delinsGCT NCBI36
NG_008377.1:g.7454_7456delinsAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.654+225_654+227delinsAGC MANE Select ENSP00000301141.4:n.654+225_654+227delinsAGC
ENST00000301141.9:c.654+225_654+227delinsAGC ENSP00000301141.4:n.654+225_654+227delinsAGC
ENST00000596719.5:n.505+225_505+227delinsAGC
ENST00000600495.1:c.*466+225_*466+227delinsAGC ENSP00000472905.1:n.*466+225_*466+227delinsAGC
ENST00000601627.1:c.120-43999_120-43997delinsGCT
ENST00000610301.1:c.654+225_654+227delinsAGC ENSP00000477899.1:n.654+225_654+227delinsAGC
NM_000762.5:c.654+225_654+227delinsAGC NP_000753.3:n.654+225_654+227delinsAGC
NM_000762.6:c.654+225_654+227delinsAGC MANE Select NP_000753.3:n.654+225_654+227delinsAGC