Canonical Allele Identifier: CA2335910055
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs2077497875

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285371_40285377dup , CM000681.2:g.40285371_40285377dup GRCh38
NC_000019.9:g.40791278_40791284dup , CM000681.1:g.40791278_40791284dup GRCh37
NC_000019.8:g.45483118_45483124dup NCBI36
NG_012038.2:g.4987_4993dup

Transcript Alleles

HGVS Amino-acid change
ENST00000392038.6:c.-276_-270dup ENSP00000375892.2:n.-276_-270dup
ENST00000424901.5:c.-276_-270dup ENSP00000399532.2:n.-276_-270dup
ENST00000578123.5:c.-85+76_-85+82dup ENSP00000462022.1:n.-85+76_-85+82dup
NM_001243027.2:c.-425_-419dup NP_001229956.1:n.-425_-419dup
NM_001243028.2:c.-332_-326dup NP_001229957.1:n.-332_-326dup
NM_001626.5:c.-276_-270dup NP_001617.1:n.-276_-270dup
XM_011526620.1:c.-85+76_-85+82dup XP_011524922.1:n.-85+76_-85+82dup