Canonical Allele Identifier: CA2336177215
Gene: CYP2A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40845264_40845265delinsCG , CM000681.2:g.40845264_40845265delinsCG GRCh38
NC_000019.9:g.41351169_41351170delinsCG , CM000681.1:g.41351169_41351170delinsCG GRCh37
NC_000019.8:g.46043009_46043010delinsCG NCBI36
NG_008377.1:g.10183_10184delinsCG

Transcript Alleles

HGVS Amino-acid change
ENST00000301141.10:c.1161+29_1161+30delinsCG MANE Select ENSP00000301141.4:n.1161+29_1161+30delins...
ENST00000301141.9:c.1161+29_1161+30delinsCG ENSP00000301141.4:n.1161+29_1161+30delins...
ENST00000596719.5:n.1041_1042delinsCG
ENST00000601627.1:c.119+43849_119+43850delinsCG
ENST00000610301.1:c.1161+29_1161+30delinsCG ENSP00000477899.1:n.1161+29_1161+30delins...
NM_000762.5:c.1161+29_1161+30delinsCG NP_000753.3:n.1161+29_1161+30delinsCG
NM_000762.6:c.1161+29_1161+30delinsCG MANE Select NP_000753.3:n.1161+29_1161+30delinsCG