Canonical Allele Identifier: CA882232822

Gene: AKT2

Linked Data

• dbSNP Id: rs1161771213
• gnomAD v3: 19-40285331-A-AT
• gnomAD v4: 19-40285331-A-AT
• MyVariant Identifiers: chr19:g.40791238_40791239insT (hg19) ; chr19:g.40285331_40285332insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285331_40285332insT , CM000681.2:g.40285331_40285332insT	GRCh38
NC_000019.9:g.40791238_40791239insT , CM000681.1:g.40791238_40791239insT	GRCh37
NC_000019.8:g.45483078_45483079insT	NCBI36
NG_012038.2:g.5027_5028insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.-236_-235insA MANE Select	ENSP00000375892.2:n.-236_-235insA
ENST00000391844.8:c.-282_-281insA	ENSP00000375719.4:n.-282_-281insA
ENST00000392038.6:c.-236_-235insA	ENSP00000375892.2:n.-236_-235insA
ENST00000424901.5:c.-236_-235insA	ENSP00000399532.2:n.-236_-235insA
ENST00000578123.5:c.-85+116_-85+117insA	ENSP00000462022.1:n.-85+116_-85+117insA
ENST00000579047.5:c.-292_-291insA	ENSP00000471369.1:n.-292_-291insA
ENST00000584288.5:c.-375_-374insA	ENSP00000462469.1:n.-375_-374insA
NM_001243027.2:c.-385_-384insA	NP_001229956.1:n.-385_-384insA
NM_001243028.2:c.-292_-291insA	NP_001229957.1:n.-292_-291insA
NM_001626.5:c.-236_-235insA	NP_001617.1:n.-236_-235insA
XM_011526620.1:c.-85+116_-85+117insA	XP_011524922.1:n.-85+116_-85+117insA
XM_011526622.1:c.-236_-235insA	XP_011524924.1:n.-236_-235insA
XM_011526622.2:c.-236_-235insA	XP_011524924.1:n.-236_-235insA
XM_024451417.1:c.-236_-235insA	XP_024307185.1:n.-236_-235insA
NM_001626.6:c.-236_-235insA MANE Select	NP_001617.1:n.-236_-235insA
NM_001243027.3:c.-385_-384insA	NP_001229956.1:n.-385_-384insA
NM_001243028.3:c.-292_-291insA	NP_001229957.1:n.-292_-291insA