Canonical Allele Identifier: CA2585108826

Gene: AKT2

Linked Data

• gnomAD v4: 19-40285218-CTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285219_40285220del , CM000681.2:g.40285219_40285220del	GRCh38
NC_000019.9:g.40791126_40791127del , CM000681.1:g.40791126_40791127del	GRCh37
NC_000019.8:g.45482966_45482967del	NCBI36
NG_012038.2:g.5139_5140del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.-124_-123del MANE Select	ENSP00000375892.2:n.-124_-123del
ENST00000358335.9:c.-124_-123del	ENSP00000351095.5:n.-124_-123del
ENST00000391844.8:c.-170_-169del	ENSP00000375719.4:n.-170_-169del
ENST00000392038.6:c.-124_-123del	ENSP00000375892.2:n.-124_-123del
ENST00000424901.5:c.-124_-123del	ENSP00000399532.2:n.-124_-123del
ENST00000578123.5:c.-85+228_-85+229del	ENSP00000462022.1:n.-85+228_-85+229del
ENST00000579047.5:c.-180_-179del	ENSP00000471369.1:n.-180_-179del
ENST00000584288.5:c.-263_-262del	ENSP00000462469.1:n.-263_-262del
NM_001243027.2:c.-273_-272del	NP_001229956.1:n.-273_-272del
NM_001243028.2:c.-180_-179del	NP_001229957.1:n.-180_-179del
NM_001626.5:c.-124_-123del	NP_001617.1:n.-124_-123del
XM_011526620.1:c.-85+228_-85+229del	XP_011524922.1:n.-85+228_-85+229del
XM_011526622.1:c.-124_-123del	XP_011524924.1:n.-124_-123del
XM_011526622.2:c.-124_-123del	XP_011524924.1:n.-124_-123del
XM_024451417.1:c.-124_-123del	XP_024307185.1:n.-124_-123del
NM_001626.6:c.-124_-123del MANE Select	NP_001617.1:n.-124_-123del
NM_001243027.3:c.-273_-272del	NP_001229956.1:n.-273_-272del
NM_001243028.3:c.-180_-179del	NP_001229957.1:n.-180_-179del