Canonical Allele Identifier: CA2336177205
Gene: CYP2A6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40845247_40845248delinsGA , CM000681.2:g.40845247_40845248delinsGA GRCh38
NC_000019.9:g.41351152_41351153delinsGA , CM000681.1:g.41351152_41351153delinsGA GRCh37
NC_000019.8:g.46042992_46042993delinsGA NCBI36
NG_008377.1:g.10200_10201delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.1161+46_1161+47delinsTC MANE Select ENSP00000301141.4:n.1161+46_1161+47delinsTC
ENST00000301141.9:c.1161+46_1161+47delinsTC ENSP00000301141.4:n.1161+46_1161+47delinsTC
ENST00000596719.5:n.1058_1059delinsTC
ENST00000601627.1:c.119+43832_119+43833delinsGA
ENST00000610301.1:c.1161+46_1161+47delinsTC ENSP00000477899.1:n.1161+46_1161+47delinsTC
NM_000762.5:c.1161+46_1161+47delinsTC NP_000753.3:n.1161+46_1161+47delinsTC
NM_000762.6:c.1161+46_1161+47delinsTC MANE Select NP_000753.3:n.1161+46_1161+47delinsTC