Canonical Allele Identifier: CA2336178917
Gene: CYP2A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848507_40848508delinsCG , CM000681.2:g.40848507_40848508delinsCG GRCh38
NC_000019.9:g.41354412_41354413delinsCG , CM000681.1:g.41354412_41354413delinsCG GRCh37
NC_000019.8:g.46046252_46046253delinsCG NCBI36
NG_008377.1:g.6940_6941delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.493+106_493+107delinsCG MANE Select ENSP00000301141.4:n.493+106_493+107delinsCG
ENST00000301141.9:c.493+106_493+107delinsCG ENSP00000301141.4:n.493+106_493+107delinsCG
ENST00000596719.5:n.344+106_344+107delinsCG
ENST00000600495.1:c.*305+106_*305+107delinsCG ENSP00000472905.1:n.*305+106_*305+107delinsCG
ENST00000601627.1:c.120-43484_120-43483delinsCG
ENST00000610301.1:c.493+106_493+107delinsCG ENSP00000477899.1:n.493+106_493+107delinsCG
NM_000762.5:c.493+106_493+107delinsCG NP_000753.3:n.493+106_493+107delinsCG
NM_000762.6:c.493+106_493+107delinsCG MANE Select NP_000753.3:n.493+106_493+107delinsCG