Canonical Allele Identifier: CA2335909966

Gene: AKT2

Linked Data

• dbSNP Id: rs2077495381

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285297del , CM000681.2:g.40285297del	GRCh38
NC_000019.9:g.40791204del , CM000681.1:g.40791204del	GRCh37
NC_000019.8:g.45483044del	NCBI36
NG_012038.2:g.5062del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.-201del MANE Select	ENSP00000375892.2:n.-201del
ENST00000391844.8:c.-247del	ENSP00000375719.4:n.-247del
ENST00000392038.6:c.-201del	ENSP00000375892.2:n.-201del
ENST00000424901.5:c.-201del	ENSP00000399532.2:n.-201del
ENST00000578123.5:c.-85+151del	ENSP00000462022.1:n.-85+151del
ENST00000579047.5:c.-257del	ENSP00000471369.1:n.-257del
ENST00000584288.5:c.-340del	ENSP00000462469.1:n.-340del
NM_001243027.2:c.-350del	NP_001229956.1:n.-350del
NM_001243028.2:c.-257del	NP_001229957.1:n.-257del
NM_001626.5:c.-201del	NP_001617.1:n.-201del
XM_011526620.1:c.-85+151del	XP_011524922.1:n.-85+151del
XM_011526622.1:c.-201del	XP_011524924.1:n.-201del
XM_011526622.2:c.-201del	XP_011524924.1:n.-201del
XM_024451417.1:c.-201del	XP_024307185.1:n.-201del
NM_001626.6:c.-201del MANE Select	NP_001617.1:n.-201del
NM_001243027.3:c.-350del	NP_001229956.1:n.-350del
NM_001243028.3:c.-257del	NP_001229957.1:n.-257del