Canonical Allele Identifier: CA658798276

Gene: AKT1

Linked Data

• ClinVar Variation Id: 514683
• ClinVar RCV Id: RCV000606636 ; RCV001229553
• dbSNP Id: rs1219173005
• MyVariant Identifiers: chr14:g.105239585C>T (hg19) ; chr14:g.104773248C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104773248C>T , CM000676.2:g.104773248C>T	GRCh38
NC_000014.8:g.105239585C>T , CM000676.1:g.105239585C>T	GRCh37
NC_000014.7:g.104310630C>T	NCBI36
NG_012188.1:g.27497G>A , LRG_721:g.27497G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000554192.6:c.957+3G>A	ENSP00000450681.3:n.957+3G>A
ENST00000554585.6:c.957+3G>A	ENSP00000481526.2:n.957+3G>A
ENST00000555458.6:c.957+3G>A	ENSP00000451470.3:n.957+3G>A
ENST00000553797.2:c.1032+3G>A	ENSP00000507566.1:n.1032+3G>A
ENST00000554826.2:n.1426+3G>A
ENST00000610370.2:n.1426+3G>A
ENST00000682269.1:n.1474+3G>A
ENST00000683058.1:n.834+3G>A
ENST00000683722.1:c.957+3G>A	ENSP00000507879.1:n.957+3G>A
ENST00000684058.1:n.514+3G>A
ENST00000407796.7:c.957+3G>A	ENSP00000384293.2:n.957+3G>A
ENST00000649815.2:c.957+3G>A MANE Select	ENSP00000497822.1:n.957+3G>A
ENST00000349310.7:c.957+3G>A	ENSP00000270202.4:n.957+3G>A
ENST00000402615.6:c.957+3G>A	ENSP00000385326.2:n.957+3G>A
ENST00000407796.6:c.957+3G>A	ENSP00000384293.2:n.957+3G>A
ENST00000544168.5:n.892+3G>A
ENST00000553506.5:n.1355+3G>A
ENST00000554192.5:c.166+3G>A
ENST00000554581.5:c.957+3G>A	ENSP00000451828.1:n.957+3G>A
ENST00000554585.5:c.129+3G>A	ENSP00000481526.1:n.129+3G>A
ENST00000554848.5:c.957+3G>A	ENSP00000451166.1:n.957+3G>A
ENST00000555458.5:c.64+3G>A
ENST00000555528.5:c.957+3G>A	ENSP00000450688.1:n.957+3G>A
ENST00000557552.1:n.5249G>A
NM_001014431.1:c.957+3G>A	NP_001014431.1:n.957+3G>A
NM_001014432.1:c.957+3G>A , LRG_721t1:c.957+3G>A	NP_001014432.1:n.957+3G>A
NM_005163.2:c.957+3G>A , LRG_721t2:c.957+3G>A	NP_005154.2:n.957+3G>A
XM_005267401.1:c.957+3G>A	XP_005267458.1:n.957+3G>A
XM_011536543.1:c.957+3G>A	XP_011534845.1:n.957+3G>A
XM_011536544.1:c.957+3G>A	XP_011534846.1:n.957+3G>A
XR_002957536.1:n.1157+3G>A
NM_001014431.2:c.957+3G>A	NP_001014431.1:n.957+3G>A
NM_001014432.2:c.957+3G>A	NP_001014432.1:n.957+3G>A
NM_001382430.1:c.957+3G>A MANE Select	NP_001369359.1:n.957+3G>A
NM_001382431.1:c.957+3G>A	NP_001369360.1:n.957+3G>A
NM_001382432.1:c.957+3G>A	NP_001369361.1:n.957+3G>A
NM_001382433.1:c.957+3G>A	NP_001369362.1:n.957+3G>A