Canonical Allele Identifier: CA2160960460

Gene: AKT1

Linked Data

• dbSNP Id: rs1892337389
• gnomAD v4: 14-104770710-A-AAGGGAGTGGGCGGGGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104770714_104770730dup , CM000676.2:g.104770714_104770730dup	GRCh38
NC_000014.8:g.105237051_105237067dup , CM000676.1:g.105237051_105237067dup	GRCh37
NC_000014.7:g.104308096_104308112dup	NCBI36
NG_012188.1:g.30018_30034dup , LRG_721:g.30018_30034dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000554192.6:c.1264+18_1264+34dup	ENSP00000450681.3:n.1264+18_1264+34dup
ENST00000554585.6:c.*189+18_*189+34dup	ENSP00000481526.2:n.*189+18_*189+34dup
ENST00000555458.6:c.1363+18_1363+34dup	ENSP00000451470.3:n.1363+18_1363+34dup
ENST00000553797.2:c.1438+18_1438+34dup	ENSP00000507566.1:n.1438+18_1438+34dup
ENST00000554826.2:n.1832+18_1832+34dup
ENST00000610370.2:n.3349+18_3349+34dup
ENST00000683058.1:n.1240+18_1240+34dup
ENST00000683722.1:c.1363+18_1363+34dup	ENSP00000507879.1:n.1363+18_1363+34dup
ENST00000684058.1:n.920+18_920+34dup
ENST00000407796.7:c.1363+18_1363+34dup	ENSP00000384293.2:n.1363+18_1363+34dup
ENST00000649815.2:c.1363+18_1363+34dup MANE Select	ENSP00000497822.1:n.1363+18_1363+34dup
ENST00000349310.7:c.1363+18_1363+34dup	ENSP00000270202.4:n.1363+18_1363+34dup
ENST00000402615.6:c.1363+18_1363+34dup	ENSP00000385326.2:n.1363+18_1363+34dup
ENST00000407796.6:c.1363+18_1363+34dup	ENSP00000384293.2:n.1363+18_1363+34dup
ENST00000544168.5:n.1298+18_1298+34dup
ENST00000553506.5:n.1761+18_1761+34dup
ENST00000554192.5:c.473+18_473+34dup
ENST00000554581.5:c.1363+18_1363+34dup	ENSP00000451828.1:n.1363+18_1363+34dup
ENST00000554585.5:c.630+18_630+34dup	ENSP00000481526.1:n.630+18_630+34dup
ENST00000554848.5:c.1363+18_1363+34dup	ENSP00000451166.1:n.1363+18_1363+34dup
ENST00000555458.5:c.470+18_470+34dup
ENST00000555528.5:c.1363+18_1363+34dup	ENSP00000450688.1:n.1363+18_1363+34dup
ENST00000557552.1:n.7327+18_7327+34dup
ENST00000610370.1:n.1812_1828dup
NM_001014431.1:c.1363+18_1363+34dup	NP_001014431.1:n.1363+18_1363+34dup
NM_001014432.1:c.1363+18_1363+34dup , LRG_721t1:c.1363+18_1363+34dup	NP_001014432.1:n.1363+18_1363+34dup
NM_005163.2:c.1363+18_1363+34dup , LRG_721t2:c.1363+18_1363+34dup	NP_005154.2:n.1363+18_1363+34dup
XM_005267401.1:c.1363+18_1363+34dup	XP_005267458.1:n.1363+18_1363+34dup
XM_011536543.1:c.1363+18_1363+34dup	XP_011534845.1:n.1363+18_1363+34dup
XR_002957536.1:n.3080+18_3080+34dup
NM_001014431.2:c.1363+18_1363+34dup	NP_001014431.1:n.1363+18_1363+34dup
NM_001014432.2:c.1363+18_1363+34dup	NP_001014432.1:n.1363+18_1363+34dup
NM_001382430.1:c.1363+18_1363+34dup MANE Select	NP_001369359.1:n.1363+18_1363+34dup
NM_001382431.1:c.1363+18_1363+34dup	NP_001369360.1:n.1363+18_1363+34dup
NM_001382432.1:c.1363+18_1363+34dup	NP_001369361.1:n.1363+18_1363+34dup
NM_001382433.1:c.1363+18_1363+34dup	NP_001369362.1:n.1363+18_1363+34dup