Canonical Allele Identifier: CA424353638

Gene: AKT3

Linked Data

• gnomAD v4: 1-243637617-A-G
• MyVariant Identifiers: chr1:g.243800919A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.243637617A>G , CM000663.2:g.243637617A>G	GRCh38
NC_000001.10:g.243800919A>G , CM000663.1:g.243800919A>G	GRCh37
NC_000001.9:g.241867542A>G	NCBI36
NG_029764.1:g.210968T>C
NG_029764.2:g.218463T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000263826.12:c.555T>C	ENSP00000263826.5:p.Ile185=
ENST00000366539.6:c.555T>C	ENSP00000355497.2:p.Ile185=
ENST00000492957.2:c.555T>C	ENSP00000506695.1:p.Ile185=
ENST00000672460.1:c.312T>C	ENSP00000499842.1:p.Ile104=
ENST00000672578.1:c.372T>C	ENSP00000500597.1:p.Ile124=
ENST00000673466.1:c.555T>C MANE Select	ENSP00000500582.1:p.Ile185=
ENST00000680056.1:c.429T>C	ENSP00000505337.1:p.Ile143=
ENST00000680118.1:c.555T>C	ENSP00000505276.1:p.Ile185=
ENST00000681794.1:c.555T>C	ENSP00000506399.1:p.Ile185=
ENST00000263826.9:c.555T>C	ENSP00000263826.5:p.Ile185=
ENST00000336199.9:c.555T>C	ENSP00000336943.5:p.Ile185=
ENST00000366539.5:c.555T>C	ENSP00000355497.1:p.Ile185=
ENST00000366540.5:c.555T>C	ENSP00000355498.1:p.Ile185=
NM_001206729.1:c.555T>C	NP_001193658.1:p.Ile185=
NM_005465.4:c.555T>C	NP_005456.1:p.Ile185=
NM_181690.2:c.555T>C	NP_859029.1:p.Ile185=
XM_005272994.3:c.555T>C	XP_005273051.1:p.Ile185=
XM_005272995.2:c.555T>C	XP_005273052.1:p.Ile185=
XM_005272997.3:c.372T>C	XP_005273054.1:p.Ile124=
XM_006711726.2:c.555T>C	XP_006711789.1:p.Ile185=
XM_011544011.1:c.429T>C	XP_011542313.1:p.Ile143=
XM_011544012.1:c.555T>C	XP_011542314.1:p.Ile185=
XM_011544013.1:c.555T>C	XP_011542315.1:p.Ile185=
XM_016999985.1:c.372T>C	XP_016855474.1:p.Ile124=
XM_024446000.1:c.555T>C	XP_024301768.1:p.Ile185=
XM_024446892.1:c.555T>C	XP_024302660.1:p.Ile185=
XM_024447938.1:c.555T>C	XP_024303706.1:p.Ile185=
NM_005465.5:c.555T>C	NP_005456.1:p.Ile185=
NM_001370074.1:c.555T>C	NP_001357003.1:p.Ile185=
NM_005465.7:c.555T>C MANE Select	NP_005456.1:p.Ile185=
NM_001206729.2:c.555T>C	NP_001193658.1:p.Ile185=