Canonical Allele Identifier: CA2336177054
Gene: CYP2A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40844999_40845000delinsAC , CM000681.2:g.40844999_40845000delinsAC GRCh38
NC_000019.9:g.41350904_41350905delinsAC , CM000681.1:g.41350904_41350905delinsAC GRCh37
NC_000019.8:g.46042744_46042745delinsAC NCBI36
NG_008377.1:g.10448_10449delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.1162-228_1162-227delinsGT MANE Select ENSP00000301141.4:n.1162-228_1162-227delinsGT
ENST00000301141.9:c.1162-228_1162-227delinsGT ENSP00000301141.4:n.1162-228_1162-227delinsGT
ENST00000596719.5:n.1306_1307delinsGT
ENST00000601627.1:c.119+43584_119+43585delinsAC
ENST00000610301.1:c.1162-228_1162-227delinsGT ENSP00000477899.1:n.1162-228_1162-227delinsGT
NM_000762.5:c.1162-228_1162-227delinsGT NP_000753.3:n.1162-228_1162-227delinsGT
NM_000762.6:c.1162-228_1162-227delinsGT MANE Select NP_000753.3:n.1162-228_1162-227delinsGT