Canonical Allele Identifier: CA2335910019

Gene: AKT2

Linked Data

• dbSNP Id: rs2077496835

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285347_40285348del , CM000681.2:g.40285347_40285348del	GRCh38
NC_000019.9:g.40791254_40791255del , CM000681.1:g.40791254_40791255del	GRCh37
NC_000019.8:g.45483094_45483095del	NCBI36
NG_012038.2:g.5014_5015del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391844.8:c.-295_-294del	ENSP00000375719.4:n.-295_-294del
ENST00000392038.6:c.-249_-248del	ENSP00000375892.2:n.-249_-248del
ENST00000424901.5:c.-249_-248del	ENSP00000399532.2:n.-249_-248del
ENST00000578123.5:c.-85+103_-85+104del	ENSP00000462022.1:n.-85+103_-85+104del
NM_001243027.2:c.-398_-397del	NP_001229956.1:n.-398_-397del
NM_001243028.2:c.-305_-304del	NP_001229957.1:n.-305_-304del
NM_001626.5:c.-249_-248del	NP_001617.1:n.-249_-248del
XM_011526620.1:c.-85+103_-85+104del	XP_011524922.1:n.-85+103_-85+104del