Canonical Allele Identifier: CA16042842

Gene: AKT1

Linked Data

• ClinVar Variation Id: 373773
• ClinVar RCV Id: RCV000413604 ; RCV001851003
• dbSNP Id: rs1057518602
• MyVariant Identifiers: chr14:g.105243047T>C (hg19) ; chr14:g.104776710T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104776710T>C , CM000676.2:g.104776710T>C	GRCh38
NC_000014.8:g.105243047T>C , CM000676.1:g.105243047T>C	GRCh37
NC_000014.7:g.104314092T>C	NCBI36
NG_012188.1:g.24035A>G , LRG_721:g.24035A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000554192.6:c.236A>G	ENSP00000450681.3:p.Gln79Arg
ENST00000554585.6:c.236A>G	ENSP00000481526.2:p.Gln79Arg
ENST00000555458.6:c.236A>G	ENSP00000451470.3:p.Gln79Arg
ENST00000553797.2:c.236A>G	ENSP00000507566.1:p.Gln79Arg
ENST00000554826.2:n.374A>G
ENST00000610370.2:n.374A>G
ENST00000682269.1:n.753A>G
ENST00000683722.1:c.236A>G	ENSP00000507879.1:p.Gln79Arg
ENST00000407796.7:c.236A>G	ENSP00000384293.2:p.Gln79Arg
ENST00000649815.2:c.236A>G MANE Select	ENSP00000497822.1:p.Gln79Arg
ENST00000349310.7:c.236A>G	ENSP00000270202.4:p.Gln79Arg
ENST00000402615.6:c.236A>G	ENSP00000385326.2:p.Gln79Arg
ENST00000407796.6:c.236A>G	ENSP00000384293.2:p.Gln79Arg
ENST00000544168.5:n.171A>G
ENST00000554581.5:c.236A>G	ENSP00000451828.1:p.Gln79Arg
ENST00000554848.5:c.236A>G	ENSP00000451166.1:p.Gln79Arg
ENST00000555380.1:n.267A>G
ENST00000555528.5:c.236A>G	ENSP00000450688.1:p.Gln79Arg
ENST00000555926.1:c.236A>G	ENSP00000451824.1:p.Gln79Arg
ENST00000557552.1:n.1862A>G
NM_001014431.1:c.236A>G	NP_001014431.1:p.Gln79Arg
NM_001014432.1:c.236A>G , LRG_721t1:c.236A>G	NP_001014432.1:p.Gln79Arg
NM_005163.2:c.236A>G , LRG_721t2:c.236A>G	NP_005154.2:p.Gln79Arg
XM_005267401.1:c.236A>G	XP_005267458.1:p.Gln79Arg
XM_011536543.1:c.236A>G	XP_011534845.1:p.Gln79Arg
XM_011536544.1:c.236A>G	XP_011534846.1:p.Gln79Arg
XR_002957536.1:n.436A>G
NM_001014431.2:c.236A>G	NP_001014431.1:p.Gln79Arg
NM_001014432.2:c.236A>G	NP_001014432.1:p.Gln79Arg
NM_001382430.1:c.236A>G MANE Select	NP_001369359.1:p.Gln79Arg
NM_001382431.1:c.236A>G	NP_001369360.1:p.Gln79Arg
NM_001382432.1:c.236A>G	NP_001369361.1:p.Gln79Arg
NM_001382433.1:c.236A>G	NP_001369362.1:p.Gln79Arg