Canonical Allele Identifier: CA2336177049
Gene: CYP2A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40844993_40844994delinsTG , CM000681.2:g.40844993_40844994delinsTG GRCh38
NC_000019.9:g.41350898_41350899delinsTG , CM000681.1:g.41350898_41350899delinsTG GRCh37
NC_000019.8:g.46042738_46042739delinsTG NCBI36
NG_008377.1:g.10454_10455delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.1162-222_1162-221delinsCA MANE Select ENSP00000301141.4:n.1162-222_1162-221delinsCA
ENST00000301141.9:c.1162-222_1162-221delinsCA ENSP00000301141.4:n.1162-222_1162-221delinsCA
ENST00000596719.5:n.1312_1313delinsCA
ENST00000601627.1:c.119+43578_119+43579delinsTG
ENST00000610301.1:c.1162-222_1162-221delinsCA ENSP00000477899.1:n.1162-222_1162-221delinsCA
NM_000762.5:c.1162-222_1162-221delinsCA NP_000753.3:n.1162-222_1162-221delinsCA
NM_000762.6:c.1162-222_1162-221delinsCA MANE Select NP_000753.3:n.1162-222_1162-221delinsCA