Canonical Allele Identifier: CA7374436

Gene: AKT1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104770359C>T , CM000676.2:g.104770359C>T	GRCh38
NC_000014.8:g.105236696C>T , CM000676.1:g.105236696C>T	GRCh37
NC_000014.7:g.104307741C>T	NCBI36
NG_012188.1:g.30386G>A , LRG_721:g.30386G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001382430.1:c.1425G>A MANE Select	NP_001369359.1:p.Ser475=
ENST00000649815.2:c.1425G>A MANE Select	ENSP00000497822.1:p.Ser475=
NM_001014431.1:c.1425G>A	NP_001014431.1:p.Ser475=
NM_001014431.2:c.1425G>A	NP_001014431.1:p.Ser475=
NM_001014432.1:c.1425G>A , LRG_721t1:c.1425G>A	NP_001014432.1:p.Ser475=
NM_001014432.2:c.1425G>A	NP_001014432.1:p.Ser475=
NM_001382431.1:c.1425G>A	NP_001369360.1:p.Ser475=
NM_001382432.1:c.1425G>A	NP_001369361.1:p.Ser475=
NM_001382433.1:c.1425G>A	NP_001369362.1:p.Ser475=
NM_005163.2:c.1425G>A , LRG_721t2:c.1425G>A	NP_005154.2:p.Ser475=
ENST00000349310.7:c.1425G>A	ENSP00000270202.4:p.Ser475=
ENST00000402615.6:c.1425G>A	ENSP00000385326.2:p.Ser475=
ENST00000407796.6:c.1425G>A	ENSP00000384293.2:p.Ser475=
ENST00000407796.7:c.1425G>A	ENSP00000384293.2:p.Ser475=
ENST00000544168.5:n.1360G>A
ENST00000553506.5:n.1823G>A
ENST00000553797.2:c.1500G>A	ENSP00000507566.1:p.Ser500=
ENST00000554192.5:c.535G>A
ENST00000554192.6:c.1326G>A	ENSP00000450681.3:p.Ser442=
ENST00000554581.5:c.1425G>A	ENSP00000451828.1:p.Ser475=
ENST00000554585.5:c.692G>A	ENSP00000481526.1:n.692G>A
ENST00000554585.6:c.*251G>A	ENSP00000481526.2:n.*251G>A
ENST00000554826.2:n.1894G>A
ENST00000554848.5:c.1425G>A	ENSP00000451166.1:p.Ser475=
ENST00000555458.5:c.470+386G>A
ENST00000555458.6:c.1363+386G>A	ENSP00000451470.3:n.1363+386G>A
ENST00000555528.5:c.1425G>A	ENSP00000450688.1:p.Ser475=
ENST00000557552.1:n.7389G>A
ENST00000610370.1:n.2180G>A
ENST00000610370.2:n.3411G>A
ENST00000683058.1:n.1302G>A
ENST00000683722.1:c.1425G>A	ENSP00000507879.1:p.Ser475=
ENST00000684058.1:n.982G>A
XM_005267401.1:c.1425G>A	XP_005267458.1:p.Ser475=
XM_011536543.1:c.1425G>A	XP_011534845.1:p.Ser475=
XR_002957536.1:n.3142G>A