Canonical Allele Identifier: CA995878710
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs2077497843

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285366_40285379dup , CM000681.2:g.40285366_40285379dup GRCh38
NC_000019.9:g.40791273_40791286dup , CM000681.1:g.40791273_40791286dup GRCh37
NC_000019.8:g.45483113_45483126dup NCBI36
NG_012038.2:g.4981_4994dup

Transcript Alleles

HGVS Amino-acid change
ENST00000392038.6:c.-282_-269dup ENSP00000375892.2:n.-282_-269dup
ENST00000424901.5:c.-282_-269dup ENSP00000399532.2:n.-282_-269dup
ENST00000578123.5:c.-85+70_-85+83dup ENSP00000462022.1:n.-85+70_-85+83dup
NM_001243027.2:c.-431_-418dup NP_001229956.1:n.-431_-418dup
NM_001243028.2:c.-338_-325dup NP_001229957.1:n.-338_-325dup
NM_001626.5:c.-282_-269dup NP_001617.1:n.-282_-269dup
XM_011526620.1:c.-85+70_-85+83dup XP_011524922.1:n.-85+70_-85+83dup