Canonical Allele Identifier: CA2585205123
Gene: CYP2A6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848564_40848586del , CM000681.2:g.40848564_40848586del GRCh38
NC_000019.9:g.41354469_41354491del , CM000681.1:g.41354469_41354491del GRCh37
NC_000019.8:g.46046309_46046331del NCBI36
NG_008377.1:g.6863_6885del

Transcript Alleles

HGVS Amino-acid change
ENST00000301141.10:c.493+29_493+51del MANE Select ENSP00000301141.4:n.493+29_493+51del
ENST00000301141.9:c.493+29_493+51del ENSP00000301141.4:n.493+29_493+51del
ENST00000596719.5:n.344+29_344+51del
ENST00000600495.1:c.*305+29_*305+51del ENSP00000472905.1:n.*305+29_*305+51del
ENST00000601627.1:c.120-43427_120-43405del
ENST00000610301.1:c.493+29_493+51del ENSP00000477899.1:n.493+29_493+51del
NM_000762.5:c.493+29_493+51del NP_000753.3:n.493+29_493+51del
NM_000762.6:c.493+29_493+51del MANE Select NP_000753.3:n.493+29_493+51del