Canonical Allele Identifier: CA424353707
Gene: AKT3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.243800988A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.243637686A>C , CM000663.2:g.243637686A>C GRCh38
NC_000001.10:g.243800988A>C , CM000663.1:g.243800988A>C GRCh37
NC_000001.9:g.241867611A>C NCBI36
NG_029764.1:g.210899T>G
NG_029764.2:g.218394T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263826.12:c.486T>G ENSP00000263826.5:p.Val162=
ENST00000366539.6:c.486T>G ENSP00000355497.2:p.Val162=
ENST00000492957.2:c.486T>G ENSP00000506695.1:p.Val162=
ENST00000672460.1:c.243T>G ENSP00000499842.1:p.Val81=
ENST00000672578.1:c.303T>G ENSP00000500597.1:p.Val101=
ENST00000673466.1:c.486T>G MANE Select ENSP00000500582.1:p.Val162=
ENST00000680056.1:c.360T>G ENSP00000505337.1:p.Val120=
ENST00000680118.1:c.486T>G ENSP00000505276.1:p.Val162=
ENST00000681794.1:c.486T>G ENSP00000506399.1:p.Val162=
ENST00000263826.9:c.486T>G ENSP00000263826.5:p.Val162=
ENST00000336199.9:c.486T>G ENSP00000336943.5:p.Val162=
ENST00000366539.5:c.486T>G ENSP00000355497.1:p.Val162=
ENST00000366540.5:c.486T>G ENSP00000355498.1:p.Val162=
NM_001206729.1:c.486T>G NP_001193658.1:p.Val162=
NM_005465.4:c.486T>G NP_005456.1:p.Val162=
NM_181690.2:c.486T>G NP_859029.1:p.Val162=
XM_005272994.3:c.486T>G XP_005273051.1:p.Val162=
XM_005272995.2:c.486T>G XP_005273052.1:p.Val162=
XM_005272997.3:c.303T>G XP_005273054.1:p.Val101=
XM_006711726.2:c.486T>G XP_006711789.1:p.Val162=
XM_011544011.1:c.360T>G XP_011542313.1:p.Val120=
XM_011544012.1:c.486T>G XP_011542314.1:p.Val162=
XM_011544013.1:c.486T>G XP_011542315.1:p.Val162=
XM_016999985.1:c.303T>G XP_016855474.1:p.Val101=
XM_024446000.1:c.486T>G XP_024301768.1:p.Val162=
XM_024446892.1:c.486T>G XP_024302660.1:p.Val162=
XM_024447938.1:c.486T>G XP_024303706.1:p.Val162=
NM_005465.5:c.486T>G NP_005456.1:p.Val162=
NM_001370074.1:c.486T>G NP_001357003.1:p.Val162=
NM_005465.7:c.486T>G MANE Select NP_005456.1:p.Val162=
NM_001206729.2:c.486T>G NP_001193658.1:p.Val162=
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