Canonical Allele Identifier: CA424353727

Gene: AKT3

Linked Data

• gnomAD v4: 1-243637701-G-T
• MyVariant Identifiers: chr1:g.243801003G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243637701G>T , CM000663.2:g.243637701G>T	GRCh38
NC_000001.10:g.243801003G>T , CM000663.1:g.243801003G>T	GRCh37
NC_000001.9:g.241867626G>T	NCBI36
NG_029764.1:g.210884C>A
NG_029764.2:g.218379C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000263826.12:c.471C>A	ENSP00000263826.5:p.Gly157=
ENST00000366539.6:c.471C>A	ENSP00000355497.2:p.Gly157=
ENST00000492957.2:c.471C>A	ENSP00000506695.1:p.Gly157=
ENST00000672460.1:c.228C>A	ENSP00000499842.1:p.Gly76=
ENST00000672578.1:c.288C>A	ENSP00000500597.1:p.Gly96=
ENST00000673466.1:c.471C>A MANE Select	ENSP00000500582.1:p.Gly157=
ENST00000680056.1:c.345C>A	ENSP00000505337.1:p.Gly115=
ENST00000680118.1:c.471C>A	ENSP00000505276.1:p.Gly157=
ENST00000681794.1:c.471C>A	ENSP00000506399.1:p.Gly157=
ENST00000263826.9:c.471C>A	ENSP00000263826.5:p.Gly157=
ENST00000336199.9:c.471C>A	ENSP00000336943.5:p.Gly157=
ENST00000366539.5:c.471C>A	ENSP00000355497.1:p.Gly157=
ENST00000366540.5:c.471C>A	ENSP00000355498.1:p.Gly157=
NM_001206729.1:c.471C>A	NP_001193658.1:p.Gly157=
NM_005465.4:c.471C>A	NP_005456.1:p.Gly157=
NM_181690.2:c.471C>A	NP_859029.1:p.Gly157=
XM_005272994.3:c.471C>A	XP_005273051.1:p.Gly157=
XM_005272995.2:c.471C>A	XP_005273052.1:p.Gly157=
XM_005272997.3:c.288C>A	XP_005273054.1:p.Gly96=
XM_006711726.2:c.471C>A	XP_006711789.1:p.Gly157=
XM_011544011.1:c.345C>A	XP_011542313.1:p.Gly115=
XM_011544012.1:c.471C>A	XP_011542314.1:p.Gly157=
XM_011544013.1:c.471C>A	XP_011542315.1:p.Gly157=
XM_016999985.1:c.288C>A	XP_016855474.1:p.Gly96=
XM_024446000.1:c.471C>A	XP_024301768.1:p.Gly157=
XM_024446892.1:c.471C>A	XP_024302660.1:p.Gly157=
XM_024447938.1:c.471C>A	XP_024303706.1:p.Gly157=
NM_005465.5:c.471C>A	NP_005456.1:p.Gly157=
NM_001370074.1:c.471C>A	NP_001357003.1:p.Gly157=
NM_005465.7:c.471C>A MANE Select	NP_005456.1:p.Gly157=
NM_001206729.2:c.471C>A	NP_001193658.1:p.Gly157=