Canonical Allele Identifier: CA2335910015

Gene: AKT2

Linked Data

• dbSNP Id: rs2077496752
• gnomAD v4: 19-40285342-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285342C>G , CM000681.2:g.40285342C>G	GRCh38
NC_000019.9:g.40791249C>G , CM000681.1:g.40791249C>G	GRCh37
NC_000019.8:g.45483089C>G	NCBI36
NG_012038.2:g.5017G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.-246G>C MANE Select	ENSP00000375892.2:n.-246G>C
ENST00000391844.8:c.-292G>C	ENSP00000375719.4:n.-292G>C
ENST00000392038.6:c.-246G>C	ENSP00000375892.2:n.-246G>C
ENST00000424901.5:c.-246G>C	ENSP00000399532.2:n.-246G>C
ENST00000578123.5:c.-85+106G>C	ENSP00000462022.1:n.-85+106G>C
ENST00000579047.5:c.-302G>C	ENSP00000471369.1:n.-302G>C
ENST00000584288.5:c.-385G>C	ENSP00000462469.1:n.-385G>C
NM_001243027.2:c.-395G>C	NP_001229956.1:n.-395G>C
NM_001243028.2:c.-302G>C	NP_001229957.1:n.-302G>C
NM_001626.5:c.-246G>C	NP_001617.1:n.-246G>C
XM_011526620.1:c.-85+106G>C	XP_011524922.1:n.-85+106G>C
XM_011526622.1:c.-246G>C	XP_011524924.1:n.-246G>C
XM_011526622.2:c.-246G>C	XP_011524924.1:n.-246G>C
XM_024451417.1:c.-246G>C	XP_024307185.1:n.-246G>C
NM_001626.6:c.-246G>C MANE Select	NP_001617.1:n.-246G>C
NM_001243027.3:c.-395G>C	NP_001229956.1:n.-395G>C
NM_001243028.3:c.-302G>C	NP_001229957.1:n.-302G>C