Canonical Allele Identifier: CA7374459

Gene: AKT1

Linked Data

• dbSNP Id: rs757685843
• ExAC: 14:105237044 GAA / G
• gnomAD v2: 14-105237044-GAA-G
• gnomAD v3: 14-104770707-GAA-G
• gnomAD v4: 14-104770707-GAA-G
• MyVariant Identifiers: chr14:g.105237045_105237046del (hg19) ; chr14:g.104770708_104770709del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104770710_104770711del , CM000676.2:g.104770710_104770711del	GRCh38
NC_000014.8:g.105237047_105237048del , CM000676.1:g.105237047_105237048del	GRCh37
NC_000014.7:g.104308092_104308093del	NCBI36
NG_012188.1:g.30036_30037del , LRG_721:g.30036_30037del

Transcript Alleles

HGVS	Amino-acid change
ENST00000554192.6:c.1264+36_1264+37del	ENSP00000450681.3:n.1264+36_1264+37del
ENST00000554585.6:c.*189+36_*189+37del	ENSP00000481526.2:n.*189+36_*189+37del
ENST00000555458.6:c.1363+36_1363+37del	ENSP00000451470.3:n.1363+36_1363+37del
ENST00000553797.2:c.1438+36_1438+37del	ENSP00000507566.1:n.1438+36_1438+37del
ENST00000554826.2:n.1832+36_1832+37del
ENST00000610370.2:n.3349+36_3349+37del
ENST00000683058.1:n.1240+36_1240+37del
ENST00000683722.1:c.1363+36_1363+37del	ENSP00000507879.1:n.1363+36_1363+37del
ENST00000684058.1:n.920+36_920+37del
ENST00000407796.7:c.1363+36_1363+37del	ENSP00000384293.2:n.1363+36_1363+37del
ENST00000649815.2:c.1363+36_1363+37del MANE Select	ENSP00000497822.1:n.1363+36_1363+37del
ENST00000349310.7:c.1363+36_1363+37del	ENSP00000270202.4:n.1363+36_1363+37del
ENST00000402615.6:c.1363+36_1363+37del	ENSP00000385326.2:n.1363+36_1363+37del
ENST00000407796.6:c.1363+36_1363+37del	ENSP00000384293.2:n.1363+36_1363+37del
ENST00000544168.5:n.1298+36_1298+37del
ENST00000553506.5:n.1761+36_1761+37del
ENST00000554192.5:c.473+36_473+37del
ENST00000554581.5:c.1363+36_1363+37del	ENSP00000451828.1:n.1363+36_1363+37del
ENST00000554585.5:c.630+36_630+37del	ENSP00000481526.1:n.630+36_630+37del
ENST00000554848.5:c.1363+36_1363+37del	ENSP00000451166.1:n.1363+36_1363+37del
ENST00000555458.5:c.470+36_470+37del
ENST00000555528.5:c.1363+36_1363+37del	ENSP00000450688.1:n.1363+36_1363+37del
ENST00000557552.1:n.7327+36_7327+37del
ENST00000610370.1:n.1830_1831del
NM_001014431.1:c.1363+36_1363+37del	NP_001014431.1:n.1363+36_1363+37del
NM_001014432.1:c.1363+36_1363+37del , LRG_721t1:c.1363+36_1363+37del	NP_001014432.1:n.1363+36_1363+37del
NM_005163.2:c.1363+36_1363+37del , LRG_721t2:c.1363+36_1363+37del	NP_005154.2:n.1363+36_1363+37del
XM_005267401.1:c.1363+36_1363+37del	XP_005267458.1:n.1363+36_1363+37del
XM_011536543.1:c.1363+36_1363+37del	XP_011534845.1:n.1363+36_1363+37del
XR_002957536.1:n.3080+36_3080+37del
NM_001014431.2:c.1363+36_1363+37del	NP_001014431.1:n.1363+36_1363+37del
NM_001014432.2:c.1363+36_1363+37del	NP_001014432.1:n.1363+36_1363+37del
NM_001382430.1:c.1363+36_1363+37del MANE Select	NP_001369359.1:n.1363+36_1363+37del
NM_001382431.1:c.1363+36_1363+37del	NP_001369360.1:n.1363+36_1363+37del
NM_001382432.1:c.1363+36_1363+37del	NP_001369361.1:n.1363+36_1363+37del
NM_001382433.1:c.1363+36_1363+37del	NP_001369362.1:n.1363+36_1363+37del