Canonical Allele Identifier: CA2626836770

Gene: AKT1

Linked Data

• gnomAD v4: 14-104770631-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104770632_104770633del , CM000676.2:g.104770632_104770633del	GRCh38
NC_000014.8:g.105236969_105236970del , CM000676.1:g.105236969_105236970del	GRCh37
NC_000014.7:g.104308014_104308015del	NCBI36
NG_012188.1:g.30112_30113del , LRG_721:g.30112_30113del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000554192.6:c.1264+112_1264+113del	ENSP00000450681.3:n.1264+112_1264+113del
ENST00000554585.6:c.*189+112_*189+113del	ENSP00000481526.2:n.*189+112_*189+113del
ENST00000555458.6:c.1363+112_1363+113del	ENSP00000451470.3:n.1363+112_1363+113del
ENST00000553797.2:c.1438+112_1438+113del	ENSP00000507566.1:n.1438+112_1438+113del
ENST00000554826.2:n.1832+112_1832+113del
ENST00000610370.2:n.3349+112_3349+113del
ENST00000683058.1:n.1240+112_1240+113del
ENST00000683722.1:c.1363+112_1363+113del	ENSP00000507879.1:n.1363+112_1363+113del
ENST00000684058.1:n.920+112_920+113del
ENST00000407796.7:c.1363+112_1363+113del	ENSP00000384293.2:n.1363+112_1363+113del
ENST00000649815.2:c.1363+112_1363+113del MANE Select	ENSP00000497822.1:n.1363+112_1363+113del
ENST00000349310.7:c.1363+112_1363+113del	ENSP00000270202.4:n.1363+112_1363+113del
ENST00000402615.6:c.1363+112_1363+113del	ENSP00000385326.2:n.1363+112_1363+113del
ENST00000407796.6:c.1363+112_1363+113del	ENSP00000384293.2:n.1363+112_1363+113del
ENST00000544168.5:n.1298+112_1298+113del
ENST00000553506.5:n.1761+112_1761+113del
ENST00000554192.5:c.473+112_473+113del
ENST00000554581.5:c.1363+112_1363+113del	ENSP00000451828.1:n.1363+112_1363+113del
ENST00000554585.5:c.630+112_630+113del	ENSP00000481526.1:n.630+112_630+113del
ENST00000554848.5:c.1363+112_1363+113del	ENSP00000451166.1:n.1363+112_1363+113del
ENST00000555458.5:c.470+112_470+113del
ENST00000555528.5:c.1363+112_1363+113del	ENSP00000450688.1:n.1363+112_1363+113del
ENST00000557552.1:n.7327+112_7327+113del
ENST00000610370.1:n.1906_1907del
NM_001014431.1:c.1363+112_1363+113del	NP_001014431.1:n.1363+112_1363+113del
NM_001014432.1:c.1363+112_1363+113del , LRG_721t1:c.1363+112_1363+113del	NP_001014432.1:n.1363+112_1363+113del
NM_005163.2:c.1363+112_1363+113del , LRG_721t2:c.1363+112_1363+113del	NP_005154.2:n.1363+112_1363+113del
XM_005267401.1:c.1363+112_1363+113del	XP_005267458.1:n.1363+112_1363+113del
XM_011536543.1:c.1363+112_1363+113del	XP_011534845.1:n.1363+112_1363+113del
XR_002957536.1:n.3080+112_3080+113del
NM_001014431.2:c.1363+112_1363+113del	NP_001014431.1:n.1363+112_1363+113del
NM_001014432.2:c.1363+112_1363+113del	NP_001014432.1:n.1363+112_1363+113del
NM_001382430.1:c.1363+112_1363+113del MANE Select	NP_001369359.1:n.1363+112_1363+113del
NM_001382431.1:c.1363+112_1363+113del	NP_001369360.1:n.1363+112_1363+113del
NM_001382432.1:c.1363+112_1363+113del	NP_001369361.1:n.1363+112_1363+113del
NM_001382433.1:c.1363+112_1363+113del	NP_001369362.1:n.1363+112_1363+113del