Canonical Allele Identifier: CA2626841276

Gene: AKT1

Linked Data

• gnomAD v4: 14-104793299-C-CTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104793299_104793300insTGT , CM000676.2:g.104793299_104793300insTGT	GRCh38
NC_000014.8:g.105259636_105259637insTGT , CM000676.1:g.105259636_105259637insTGT	GRCh37
NC_000014.7:g.104330681_104330682insTGT	NCBI36
NG_012188.1:g.7445_7446insACA , LRG_721:g.7445_7446insACA

Transcript Alleles

HGVS	Amino-acid change
ENST00000554192.6:c.-79-578_-79-577insACA	ENSP00000450681.3:n.-79-578_-79-577insACA...
ENST00000554585.6:c.-79-578_-79-577insACA	ENSP00000481526.2:n.-79-578_-79-577insACA...
ENST00000555458.6:c.-79-578_-79-577insACA	ENSP00000451470.3:n.-79-578_-79-577insACA...
ENST00000553797.2:c.-253_-252insACA	ENSP00000507566.1:n.-253_-252insACA
ENST00000554826.2:n.60-578_60-577insACA
ENST00000610370.2:n.60-578_60-577insACA
ENST00000682269.1:n.265_266insACA
ENST00000683722.1:c.-79-578_-79-577insACA	ENSP00000507879.1:n.-79-578_-79-577insACA...
ENST00000407796.7:c.-79-578_-79-577insACA	ENSP00000384293.2:n.-79-578_-79-577insACA...
ENST00000649815.2:c.-253_-252insACA MANE Select	ENSP00000497822.1:n.-253_-252insACA
ENST00000349310.7:c.-163-90_-163-89insACA	ENSP00000270202.4:n.-163-90_-163-89insACA...
ENST00000402615.6:c.-253_-252insACA	ENSP00000385326.2:n.-253_-252insACA
ENST00000407796.6:c.-79-578_-79-577insACA	ENSP00000384293.2:n.-79-578_-79-577insACA...
ENST00000554581.5:c.-657_-656insACA	ENSP00000451828.1:n.-657_-656insACA
ENST00000554848.5:c.-79-578_-79-577insACA	ENSP00000451166.1:n.-79-578_-79-577insACA...
ENST00000555528.5:c.-253_-252insACA	ENSP00000450688.1:n.-253_-252insACA
ENST00000555926.1:c.-253_-252insACA	ENSP00000451824.1:n.-253_-252insACA
ENST00000557494.1:n.265_266insACA
NM_001014431.1:c.-79-578_-79-577insACA	NP_001014431.1:n.-79-578_-79-577insACA
NM_001014432.1:c.-163-90_-163-89insACA , LRG_721t1:c.-163-90_-163-89insACA	NP_001014432.1:n.-163-90_-163-89insACA
NM_005163.2:c.-253_-252insACA , LRG_721t2:c.-253_-252insACA	NP_005154.2:n.-253_-252insACA
XM_005267401.1:c.-79-578_-79-577insACA	XP_005267458.1:n.-79-578_-79-577insACA
XM_011536543.1:c.-253_-252insACA	XP_011534845.1:n.-253_-252insACA
XM_011536544.1:c.-253_-252insACA	XP_011534846.1:n.-253_-252insACA
XR_002957536.1:n.38-90_38-89insACA
NM_001014431.2:c.-79-578_-79-577insACA	NP_001014431.1:n.-79-578_-79-577insACA
NM_001014432.2:c.-163-90_-163-89insACA	NP_001014432.1:n.-163-90_-163-89insACA
NM_001382430.1:c.-253_-252insACA MANE Select	NP_001369359.1:n.-253_-252insACA
NM_001382431.1:c.-79-578_-79-577insACA	NP_001369360.1:n.-79-578_-79-577insACA
NM_001382432.1:c.-163-90_-163-89insACA	NP_001369361.1:n.-163-90_-163-89insACA
NM_001382433.1:c.-253_-252insACA	NP_001369362.1:n.-253_-252insACA