Canonical Allele Identifier: CA995878676

Gene: AKT2

Linked Data

• dbSNP Id: rs2077497376
• gnomAD v3: 19-40285355-C-CA
• gnomAD v4: 19-40285355-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285355_40285356insA , CM000681.2:g.40285355_40285356insA	GRCh38
NC_000019.9:g.40791262_40791263insA , CM000681.1:g.40791262_40791263insA	GRCh37
NC_000019.8:g.45483102_45483103insA	NCBI36
NG_012038.2:g.5003_5004insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391844.8:c.-306_-305insT	ENSP00000375719.4:n.-306_-305insT
ENST00000392038.6:c.-260_-259insT	ENSP00000375892.2:n.-260_-259insT
ENST00000424901.5:c.-260_-259insT	ENSP00000399532.2:n.-260_-259insT
ENST00000578123.5:c.-85+92_-85+93insT	ENSP00000462022.1:n.-85+92_-85+93insT
NM_001243027.2:c.-409_-408insT	NP_001229956.1:n.-409_-408insT
NM_001243028.2:c.-316_-315insT	NP_001229957.1:n.-316_-315insT
NM_001626.5:c.-260_-259insT	NP_001617.1:n.-260_-259insT
XM_011526620.1:c.-85+92_-85+93insT	XP_011524922.1:n.-85+92_-85+93insT