Canonical Allele Identifier: CA995878691

Gene: AKT2

Linked Data

• dbSNP Id: rs1224933223
• gnomAD v3: 19-40285358-G-GCCCCCTCCCCCT
• gnomAD v4: 19-40285358-G-GCCCCCTCCCCCT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285369_40285370insTCCCCCTCCCCC , CM000681.2:g.40285369_40285370insTCCCCCTCCCCC	GRCh38
NC_000019.9:g.40791276_40791277insTCCCCCTCCCCC , CM000681.1:g.40791276_40791277insTCCCCCTCCCCC	GRCh37
NC_000019.8:g.45483116_45483117insTCCCCCTCCCCC	NCBI36
NG_012038.2:g.5000_5001insAGGGGGAGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391844.8:c.-309_-308insAGGGGGAGGGGG	ENSP00000375719.4:n.-309_-308insAGGGGGAGGGGG
ENST00000392038.6:c.-263_-262insAGGGGGAGGGGG	ENSP00000375892.2:n.-263_-262insAGGGGGAGGGGG
ENST00000424901.5:c.-263_-262insAGGGGGAGGGGG	ENSP00000399532.2:n.-263_-262insAGGGGGAGGGGG
ENST00000578123.5:c.-85+89_-85+90insAGGGGGAGGGGG	ENSP00000462022.1:n.-85+89_-85+90insAGGGGGAGGGGG
NM_001243027.2:c.-412_-411insAGGGGGAGGGGG	NP_001229956.1:n.-412_-411insAGGGGGAGGGGG
NM_001243028.2:c.-319_-318insAGGGGGAGGGGG	NP_001229957.1:n.-319_-318insAGGGGGAGGGGG
NM_001626.5:c.-263_-262insAGGGGGAGGGGG	NP_001617.1:n.-263_-262insAGGGGGAGGGGG
XM_011526620.1:c.-85+89_-85+90insAGGGGGAGGGGG	XP_011524922.1:n.-85+89_-85+90insAGGGGGAGGGGG