Canonical Allele Identifier: CA2585108813

Gene: AKT2

Linked Data

• gnomAD v4: 19-40285206-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285206T>C , CM000681.2:g.40285206T>C	GRCh38
NC_000019.9:g.40791113T>C , CM000681.1:g.40791113T>C	GRCh37
NC_000019.8:g.45482953T>C	NCBI36
NG_012038.2:g.5153A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.-110A>G MANE Select	ENSP00000375892.2:n.-110A>G
ENST00000358335.9:c.-110A>G	ENSP00000351095.5:n.-110A>G
ENST00000391844.8:c.-156A>G	ENSP00000375719.4:n.-156A>G
ENST00000392038.6:c.-110A>G	ENSP00000375892.2:n.-110A>G
ENST00000424901.5:c.-110A>G	ENSP00000399532.2:n.-110A>G
ENST00000578123.5:c.-85+242A>G	ENSP00000462022.1:n.-85+242A>G
ENST00000579047.5:c.-166A>G	ENSP00000471369.1:n.-166A>G
ENST00000584288.5:c.-249A>G	ENSP00000462469.1:n.-249A>G
NM_001243027.2:c.-259A>G	NP_001229956.1:n.-259A>G
NM_001243028.2:c.-166A>G	NP_001229957.1:n.-166A>G
NM_001626.5:c.-110A>G	NP_001617.1:n.-110A>G
XM_011526620.1:c.-85+242A>G	XP_011524922.1:n.-85+242A>G
XM_011526622.1:c.-110A>G	XP_011524924.1:n.-110A>G
XM_011526622.2:c.-110A>G	XP_011524924.1:n.-110A>G
XM_024451417.1:c.-110A>G	XP_024307185.1:n.-110A>G
NM_001626.6:c.-110A>G MANE Select	NP_001617.1:n.-110A>G
NM_001243027.3:c.-259A>G	NP_001229956.1:n.-259A>G
NM_001243028.3:c.-166A>G	NP_001229957.1:n.-166A>G