Canonical Allele Identifier: CA2336178922
Gene: CYP2A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848517_40848518delinsTC , CM000681.2:g.40848517_40848518delinsTC GRCh38
NC_000019.9:g.41354422_41354423delinsTC , CM000681.1:g.41354422_41354423delinsTC GRCh37
NC_000019.8:g.46046262_46046263delinsTC NCBI36
NG_008377.1:g.6930_6931delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.493+96_493+97delinsGA MANE Select ENSP00000301141.4:n.493+96_493+97delinsGA
ENST00000301141.9:c.493+96_493+97delinsGA ENSP00000301141.4:n.493+96_493+97delinsGA
ENST00000596719.5:n.344+96_344+97delinsGA
ENST00000600495.1:c.*305+96_*305+97delinsGA ENSP00000472905.1:n.*305+96_*305+97delinsGA
ENST00000601627.1:c.120-43474_120-43473delinsTC
ENST00000610301.1:c.493+96_493+97delinsGA ENSP00000477899.1:n.493+96_493+97delinsGA
NM_000762.5:c.493+96_493+97delinsGA NP_000753.3:n.493+96_493+97delinsGA
NM_000762.6:c.493+96_493+97delinsGA MANE Select NP_000753.3:n.493+96_493+97delinsGA