Canonical Allele Identifier: CA308416209

Gene: AKT2

Linked Data

• dbSNP Id: rs926671678
• gnomAD v2: 19-40791174-CCGGCAGCGGCAACGGCGCCGGCAG-C
• gnomAD v3: 19-40285267-CCGGCAGCGGCAACGGCGCCGGCAG-C
• gnomAD v4: 19-40285267-CCGGCAGCGGCAACGGCGCCGGCAG-C
• MyVariant Identifiers: chr19:g.40791175_40791198del (hg19) ; chr19:g.40285268_40285291del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285278_40285301del , CM000681.2:g.40285278_40285301del	GRCh38
NC_000019.9:g.40791185_40791208del , CM000681.1:g.40791185_40791208del	GRCh37
NC_000019.8:g.45483025_45483048del	NCBI36
NG_012038.2:g.5068_5091del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.-195_-172del MANE Select	ENSP00000375892.2:n.-195_-172del
ENST00000391844.8:c.-241_-218del	ENSP00000375719.4:n.-241_-218del
ENST00000392038.6:c.-195_-172del	ENSP00000375892.2:n.-195_-172del
ENST00000424901.5:c.-195_-172del	ENSP00000399532.2:n.-195_-172del
ENST00000578123.5:c.-85+157_-85+180del	ENSP00000462022.1:n.-85+157_-85+180del
ENST00000579047.5:c.-251_-228del	ENSP00000471369.1:n.-251_-228del
ENST00000584288.5:c.-334_-311del	ENSP00000462469.1:n.-334_-311del
NM_001243027.2:c.-344_-321del	NP_001229956.1:n.-344_-321del
NM_001243028.2:c.-251_-228del	NP_001229957.1:n.-251_-228del
NM_001626.5:c.-195_-172del	NP_001617.1:n.-195_-172del
XM_011526620.1:c.-85+157_-85+180del	XP_011524922.1:n.-85+157_-85+180del
XM_011526622.1:c.-195_-172del	XP_011524924.1:n.-195_-172del
XM_011526622.2:c.-195_-172del	XP_011524924.1:n.-195_-172del
XM_024451417.1:c.-195_-172del	XP_024307185.1:n.-195_-172del
NM_001626.6:c.-195_-172del MANE Select	NP_001617.1:n.-195_-172del
NM_001243027.3:c.-344_-321del	NP_001229956.1:n.-344_-321del
NM_001243028.3:c.-251_-228del	NP_001229957.1:n.-251_-228del