Canonical Allele Identifier: CA882232733

Gene: AKT2

Linked Data

• dbSNP Id: rs1283832932
• gnomAD v3: 19-40285209-G-A
• gnomAD v4: 19-40285209-G-A
• MyVariant Identifiers: chr19:g.40791116G>A (hg19) ; chr19:g.40285209G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285209G>A , CM000681.2:g.40285209G>A	GRCh38
NC_000019.9:g.40791116G>A , CM000681.1:g.40791116G>A	GRCh37
NC_000019.8:g.45482956G>A	NCBI36
NG_012038.2:g.5150C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.-113C>T MANE Select	ENSP00000375892.2:n.-113C>T
ENST00000358335.9:c.-113C>T	ENSP00000351095.5:n.-113C>T
ENST00000391844.8:c.-159C>T	ENSP00000375719.4:n.-159C>T
ENST00000392038.6:c.-113C>T	ENSP00000375892.2:n.-113C>T
ENST00000424901.5:c.-113C>T	ENSP00000399532.2:n.-113C>T
ENST00000578123.5:c.-85+239C>T	ENSP00000462022.1:n.-85+239C>T
ENST00000579047.5:c.-169C>T	ENSP00000471369.1:n.-169C>T
ENST00000584288.5:c.-252C>T	ENSP00000462469.1:n.-252C>T
NM_001243027.2:c.-262C>T	NP_001229956.1:n.-262C>T
NM_001243028.2:c.-169C>T	NP_001229957.1:n.-169C>T
NM_001626.5:c.-113C>T	NP_001617.1:n.-113C>T
XM_011526620.1:c.-85+239C>T	XP_011524922.1:n.-85+239C>T
XM_011526622.1:c.-113C>T	XP_011524924.1:n.-113C>T
XM_011526622.2:c.-113C>T	XP_011524924.1:n.-113C>T
XM_024451417.1:c.-113C>T	XP_024307185.1:n.-113C>T
NM_001626.6:c.-113C>T MANE Select	NP_001617.1:n.-113C>T
NM_001243027.3:c.-262C>T	NP_001229956.1:n.-262C>T
NM_001243028.3:c.-169C>T	NP_001229957.1:n.-169C>T