Canonical Allele Identifier: CA2160961149

Gene: AKT1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104771343G>A , CM000676.2:g.104771343G>A	GRCh38
NC_000014.8:g.105237680G>A , CM000676.1:g.105237680G>A	GRCh37
NC_000014.7:g.104308725G>A	NCBI36
NG_012188.1:g.29402C>T , LRG_721:g.29402C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000554192.6:c.1162-496C>T	ENSP00000450681.3:n.1162-496C>T
ENST00000554585.6:c.*86+379C>T	ENSP00000481526.2:n.*86+379C>T
ENST00000555458.6:c.1261-496C>T	ENSP00000451470.3:n.1261-496C>T
ENST00000553797.2:c.1336-496C>T	ENSP00000507566.1:n.1336-496C>T
ENST00000554826.2:n.1730-496C>T
ENST00000610370.2:n.2751C>T
ENST00000683058.1:n.1138-496C>T
ENST00000683722.1:c.1261-496C>T	ENSP00000507879.1:n.1261-496C>T
ENST00000684058.1:n.818-496C>T
ENST00000407796.7:c.1261-496C>T	ENSP00000384293.2:n.1261-496C>T
ENST00000649815.2:c.1261-496C>T MANE Select	ENSP00000497822.1:n.1261-496C>T
ENST00000349310.7:c.1261-496C>T	ENSP00000270202.4:n.1261-496C>T
ENST00000402615.6:c.1261-496C>T	ENSP00000385326.2:n.1261-496C>T
ENST00000407796.6:c.1261-496C>T	ENSP00000384293.2:n.1261-496C>T
ENST00000544168.5:n.1196-496C>T
ENST00000553506.5:n.1659-496C>T
ENST00000554192.5:c.371-496C>T
ENST00000554581.5:c.1261-496C>T	ENSP00000451828.1:n.1261-496C>T
ENST00000554585.5:c.527+379C>T	ENSP00000481526.1:n.527+379C>T
ENST00000554848.5:c.1261-496C>T	ENSP00000451166.1:n.1261-496C>T
ENST00000555458.5:c.368-496C>T
ENST00000555528.5:c.1261-496C>T	ENSP00000450688.1:n.1261-496C>T
ENST00000557552.1:n.6729C>T
ENST00000610370.1:n.1196C>T
NM_001014431.1:c.1261-496C>T	NP_001014431.1:n.1261-496C>T
NM_001014432.1:c.1261-496C>T , LRG_721t1:c.1261-496C>T	NP_001014432.1:n.1261-496C>T
NM_005163.2:c.1261-496C>T , LRG_721t2:c.1261-496C>T	NP_005154.2:n.1261-496C>T
XM_005267401.1:c.1261-496C>T	XP_005267458.1:n.1261-496C>T
XM_011536543.1:c.1261-496C>T	XP_011534845.1:n.1261-496C>T
XM_011536544.1:c.*465C>T	XP_011534846.1:n.*465C>T
XR_002957536.1:n.2482C>T
NM_001014431.2:c.1261-496C>T	NP_001014431.1:n.1261-496C>T
NM_001014432.2:c.1261-496C>T	NP_001014432.1:n.1261-496C>T
NM_001382430.1:c.1261-496C>T MANE Select	NP_001369359.1:n.1261-496C>T
NM_001382431.1:c.1261-496C>T	NP_001369360.1:n.1261-496C>T
NM_001382432.1:c.1261-496C>T	NP_001369361.1:n.1261-496C>T
NM_001382433.1:c.1261-496C>T	NP_001369362.1:n.1261-496C>T