Canonical Allele Identifier: CA2814387060

Gene: AKT2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285233G>C , CM000681.2:g.40285233G>C	GRCh38
NC_000019.9:g.40791140G>C , CM000681.1:g.40791140G>C	GRCh37
NC_000019.8:g.45482980G>C	NCBI36
NG_012038.2:g.5126C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.-137C>G MANE Select	ENSP00000375892.2:n.-137C>G
ENST00000358335.9:c.-137C>G	ENSP00000351095.5:n.-137C>G
ENST00000391844.8:c.-183C>G	ENSP00000375719.4:n.-183C>G
ENST00000392038.6:c.-137C>G	ENSP00000375892.2:n.-137C>G
ENST00000424901.5:c.-137C>G	ENSP00000399532.2:n.-137C>G
ENST00000578123.5:c.-85+215C>G	ENSP00000462022.1:n.-85+215C>G
ENST00000579047.5:c.-193C>G	ENSP00000471369.1:n.-193C>G
ENST00000584288.5:c.-276C>G	ENSP00000462469.1:n.-276C>G
NM_001243027.2:c.-286C>G	NP_001229956.1:n.-286C>G
NM_001243028.2:c.-193C>G	NP_001229957.1:n.-193C>G
NM_001626.5:c.-137C>G	NP_001617.1:n.-137C>G
XM_011526620.1:c.-85+215C>G	XP_011524922.1:n.-85+215C>G
XM_011526622.1:c.-137C>G	XP_011524924.1:n.-137C>G
XM_011526622.2:c.-137C>G	XP_011524924.1:n.-137C>G
XM_024451417.1:c.-137C>G	XP_024307185.1:n.-137C>G
NM_001626.6:c.-137C>G MANE Select	NP_001617.1:n.-137C>G
NM_001243027.3:c.-286C>G	NP_001229956.1:n.-286C>G
NM_001243028.3:c.-193C>G	NP_001229957.1:n.-193C>G