Canonical Allele Identifier: CA2160960455

Gene: AKT1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104770707_104770709delinsGAA , CM000676.2:g.104770707_104770709delinsGAA	GRCh38
NC_000014.8:g.105237044_105237046delinsGAA , CM000676.1:g.105237044_105237046delinsGAA	GRCh37
NC_000014.7:g.104308089_104308091delinsGAA	NCBI36
NG_012188.1:g.30036_30038delinsTTC , LRG_721:g.30036_30038delinsTTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000554192.6:c.1264+36_1264+38delinsTTC	ENSP00000450681.3:n.1264+36_1264+38delins...
ENST00000554585.6:c.*189+36_*189+38delinsTTC	ENSP00000481526.2:n.*189+36_*189+38delins...
ENST00000555458.6:c.1363+36_1363+38delinsTTC	ENSP00000451470.3:n.1363+36_1363+38delins...
ENST00000553797.2:c.1438+36_1438+38delinsTTC	ENSP00000507566.1:n.1438+36_1438+38delins...
ENST00000554826.2:n.1832+36_1832+38delinsTTC
ENST00000610370.2:n.3349+36_3349+38delinsTTC
ENST00000683058.1:n.1240+36_1240+38delinsTTC
ENST00000683722.1:c.1363+36_1363+38delinsTTC	ENSP00000507879.1:n.1363+36_1363+38delins...
ENST00000684058.1:n.920+36_920+38delinsTTC
ENST00000407796.7:c.1363+36_1363+38delinsTTC	ENSP00000384293.2:n.1363+36_1363+38delins...
ENST00000649815.2:c.1363+36_1363+38delinsTTC MANE Select	ENSP00000497822.1:n.1363+36_1363+38delins...
ENST00000349310.7:c.1363+36_1363+38delinsTTC	ENSP00000270202.4:n.1363+36_1363+38delins...
ENST00000402615.6:c.1363+36_1363+38delinsTTC	ENSP00000385326.2:n.1363+36_1363+38delins...
ENST00000407796.6:c.1363+36_1363+38delinsTTC	ENSP00000384293.2:n.1363+36_1363+38delins...
ENST00000544168.5:n.1298+36_1298+38delinsTTC
ENST00000553506.5:n.1761+36_1761+38delinsTTC
ENST00000554192.5:c.473+36_473+38delinsTTC
ENST00000554581.5:c.1363+36_1363+38delinsTTC	ENSP00000451828.1:n.1363+36_1363+38delins...
ENST00000554585.5:c.630+36_630+38delinsTTC	ENSP00000481526.1:n.630+36_630+38delinsTT...
ENST00000554848.5:c.1363+36_1363+38delinsTTC	ENSP00000451166.1:n.1363+36_1363+38delins...
ENST00000555458.5:c.470+36_470+38delinsTTC
ENST00000555528.5:c.1363+36_1363+38delinsTTC	ENSP00000450688.1:n.1363+36_1363+38delins...
ENST00000557552.1:n.7327+36_7327+38delinsTTC
ENST00000610370.1:n.1830_1832delinsTTC
NM_001014431.1:c.1363+36_1363+38delinsTTC	NP_001014431.1:n.1363+36_1363+38delinsTTC...
NM_001014432.1:c.1363+36_1363+38delinsTTC , LRG_721t1:c.1363+36_1363+38delinsTTC	NP_001014432.1:n.1363+36_1363+38delinsTTC...
NM_005163.2:c.1363+36_1363+38delinsTTC , LRG_721t2:c.1363+36_1363+38delinsTTC	NP_005154.2:n.1363+36_1363+38delinsTTC
XM_005267401.1:c.1363+36_1363+38delinsTTC	XP_005267458.1:n.1363+36_1363+38delinsTTC...
XM_011536543.1:c.1363+36_1363+38delinsTTC	XP_011534845.1:n.1363+36_1363+38delinsTTC...
XR_002957536.1:n.3080+36_3080+38delinsTTC
NM_001014431.2:c.1363+36_1363+38delinsTTC	NP_001014431.1:n.1363+36_1363+38delinsTTC...
NM_001014432.2:c.1363+36_1363+38delinsTTC	NP_001014432.1:n.1363+36_1363+38delinsTTC...
NM_001382430.1:c.1363+36_1363+38delinsTTC MANE Select	NP_001369359.1:n.1363+36_1363+38delinsTTC...
NM_001382431.1:c.1363+36_1363+38delinsTTC	NP_001369360.1:n.1363+36_1363+38delinsTTC...
NM_001382432.1:c.1363+36_1363+38delinsTTC	NP_001369361.1:n.1363+36_1363+38delinsTTC...
NM_001382433.1:c.1363+36_1363+38delinsTTC	NP_001369362.1:n.1363+36_1363+38delinsTTC...