Canonical Allele Identifier: CA2585108879

Gene: AKT2

Linked Data

• dbSNP Id: rs2145449123
• gnomAD v4: 19-40285279-ACGGCGCCGGCAGCGGCAGCGGCGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285285_40285308del , CM000681.2:g.40285285_40285308del	GRCh38
NC_000019.9:g.40791192_40791215del , CM000681.1:g.40791192_40791215del	GRCh37
NC_000019.8:g.45483032_45483055del	NCBI36
NG_012038.2:g.5056_5079del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.-207_-184del MANE Select	ENSP00000375892.2:n.-207_-184del
ENST00000391844.8:c.-253_-230del	ENSP00000375719.4:n.-253_-230del
ENST00000392038.6:c.-207_-184del	ENSP00000375892.2:n.-207_-184del
ENST00000424901.5:c.-207_-184del	ENSP00000399532.2:n.-207_-184del
ENST00000578123.5:c.-85+145_-85+168del	ENSP00000462022.1:n.-85+145_-85+168del
ENST00000579047.5:c.-263_-240del	ENSP00000471369.1:n.-263_-240del
ENST00000584288.5:c.-346_-323del	ENSP00000462469.1:n.-346_-323del
NM_001243027.2:c.-356_-333del	NP_001229956.1:n.-356_-333del
NM_001243028.2:c.-263_-240del	NP_001229957.1:n.-263_-240del
NM_001626.5:c.-207_-184del	NP_001617.1:n.-207_-184del
XM_011526620.1:c.-85+145_-85+168del	XP_011524922.1:n.-85+145_-85+168del
XM_011526622.1:c.-207_-184del	XP_011524924.1:n.-207_-184del
XM_011526622.2:c.-207_-184del	XP_011524924.1:n.-207_-184del
XM_024451417.1:c.-207_-184del	XP_024307185.1:n.-207_-184del
NM_001626.6:c.-207_-184del MANE Select	NP_001617.1:n.-207_-184del
NM_001243027.3:c.-356_-333del	NP_001229956.1:n.-356_-333del
NM_001243028.3:c.-263_-240del	NP_001229957.1:n.-263_-240del