Canonical Allele Identifier: CA530268269

Gene: AKT3

Linked Data

• dbSNP Id: rs1439327545
• gnomAD v2: 1-243885811-C-T
• gnomAD v3: 1-243722509-C-T
• gnomAD v4: 1-243722509-C-T
• MyVariant Identifiers: chr1:g.243885811C>T (hg19) ; chr1:g.243722509C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243722509C>T , CM000663.2:g.243722509C>T	GRCh38
NC_000001.10:g.243885811C>T , CM000663.1:g.243885811C>T	GRCh37
NC_000001.9:g.241952434C>T	NCBI36
NG_029764.1:g.126076G>A
NG_029764.2:g.133571G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000263826.12:c.47-26793G>A	ENSP00000263826.5:n.47-26793G>A
ENST00000366539.6:c.47-26793G>A	ENSP00000355497.2:n.47-26793G>A
ENST00000491219.6:c.41-26793G>A	ENSP00000499914.1:n.41-26793G>A
ENST00000492957.2:c.47-26793G>A	ENSP00000506695.1:n.47-26793G>A
ENST00000552631.2:n.161-26793G>A
ENST00000672238.1:c.47-26793G>A	ENSP00000506535.1:n.47-26793G>A
ENST00000672442.1:c.47-26793G>A	ENSP00000500134.1:n.47-26793G>A
ENST00000672578.1:c.-137-26793G>A	ENSP00000500597.1:n.-137-26793G>A
ENST00000672679.1:n.4-26793G>A
ENST00000673400.1:c.47-26793G>A	ENSP00000504988.1:n.47-26793G>A
ENST00000673466.1:c.47-26793G>A MANE Select	ENSP00000500582.1:n.47-26793G>A
ENST00000680056.1:c.47-57626G>A	ENSP00000505337.1:n.47-57626G>A
ENST00000680118.1:c.47-26793G>A	ENSP00000505276.1:n.47-26793G>A
ENST00000681794.1:c.47-26793G>A	ENSP00000506399.1:n.47-26793G>A
ENST00000263826.9:c.47-26793G>A	ENSP00000263826.5:n.47-26793G>A
ENST00000336199.9:c.47-26793G>A	ENSP00000336943.5:n.47-26793G>A
ENST00000366539.5:c.47-26793G>A	ENSP00000355497.1:n.47-26793G>A
ENST00000366540.5:c.47-26793G>A	ENSP00000355498.1:n.47-26793G>A
ENST00000463991.5:n.185-26793G>A
ENST00000490018.1:n.538+12449G>A
ENST00000552631.1:c.47-26793G>A	ENSP00000447820.1:n.47-26793G>A
NM_001206729.1:c.47-26793G>A	NP_001193658.1:n.47-26793G>A
NM_005465.4:c.47-26793G>A	NP_005456.1:n.47-26793G>A
NM_181690.2:c.47-26793G>A	NP_859029.1:n.47-26793G>A
XM_005272994.3:c.47-26793G>A	XP_005273051.1:n.47-26793G>A
XM_005272995.2:c.47-26793G>A	XP_005273052.1:n.47-26793G>A
XM_006711726.2:c.47-26793G>A	XP_006711789.1:n.47-26793G>A
XM_011544011.1:c.47-57626G>A	XP_011542313.1:n.47-57626G>A
XM_011544012.1:c.47-26793G>A	XP_011542314.1:n.47-26793G>A
XM_011544013.1:c.47-26793G>A	XP_011542315.1:n.47-26793G>A
XM_016999985.1:c.-251-26793G>A	XP_016855474.1:n.-251-26793G>A
XM_024446000.1:c.47-26793G>A	XP_024301768.1:n.47-26793G>A
XM_024446892.1:c.47-26793G>A	XP_024302660.1:n.47-26793G>A
XM_024447938.1:c.47-26793G>A	XP_024303706.1:n.47-26793G>A
NM_005465.5:c.47-26793G>A	NP_005456.1:n.47-26793G>A
NM_001370074.1:c.47-26793G>A	NP_001357003.1:n.47-26793G>A
NM_005465.7:c.47-26793G>A MANE Select	NP_005456.1:n.47-26793G>A
NM_001206729.2:c.47-26793G>A	NP_001193658.1:n.47-26793G>A