Canonical Allele Identifier: CA633110981

Gene: AKT2

Linked Data

• dbSNP Id: rs1311906542
• gnomAD v2: 19-40791284-CGCTTA-C
• gnomAD v3: 19-40285377-CGCTTA-C
• gnomAD v4: 19-40285377-CGCTTA-C
• MyVariant Identifiers: chr19:g.40791285_40791289del (hg19) ; chr19:g.40285378_40285382del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285378_40285382del , CM000681.2:g.40285378_40285382del	GRCh38
NC_000019.9:g.40791285_40791289del , CM000681.1:g.40791285_40791289del	GRCh37
NC_000019.8:g.45483125_45483129del	NCBI36
NG_012038.2:g.4977_4981del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.6:c.-286_-282del	ENSP00000375892.2:n.-286_-282del
ENST00000424901.5:c.-286_-282del	ENSP00000399532.2:n.-286_-282del
ENST00000578123.5:c.-85+66_-85+70del	ENSP00000462022.1:n.-85+66_-85+70del
NM_001243027.2:c.-435_-431del	NP_001229956.1:n.-435_-431del
NM_001243028.2:c.-342_-338del	NP_001229957.1:n.-342_-338del
NM_001626.5:c.-286_-282del	NP_001617.1:n.-286_-282del
XM_011526620.1:c.-85+66_-85+70del	XP_011524922.1:n.-85+66_-85+70del