Canonical Allele Identifier: CA2585099775

Gene: AKT2

Linked Data

• gnomAD v4: 19-40237863-TGGGGAGCCTGGCGAATGAGGGCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40237865_40237887del , CM000681.2:g.40237865_40237887del	GRCh38
NC_000019.9:g.40743772_40743794del , CM000681.1:g.40743772_40743794del	GRCh37
NC_000019.8:g.45435612_45435634del	NCBI36
NG_012038.2:g.52473_52495del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.831+83_831+105del MANE Select	ENSP00000375892.2:n.831+83_831+105del
ENST00000578615.6:c.710+83_710+105del
ENST00000311278.10:c.831+83_831+105del	ENSP00000309428.6:n.831+83_831+105del
ENST00000391844.8:c.*445+83_*445+105del	ENSP00000375719.4:n.*445+83_*445+105del
ENST00000391845.6:n.296+83_296+105del
ENST00000392038.6:c.831+83_831+105del	ENSP00000375892.2:n.831+83_831+105del
ENST00000424901.5:c.831+83_831+105del	ENSP00000399532.2:n.831+83_831+105del
ENST00000476266.5:n.1159+83_1159+105del
ENST00000480878.6:n.258+83_258+105del
ENST00000483166.5:n.802_824del
ENST00000496089.6:n.98+83_98+105del
ENST00000578282.5:n.224+83_224+105del
ENST00000578310.1:c.75-1501_75-1479del
ENST00000578615.5:c.399+83_399+105del	ENSP00000463262.1:n.399+83_399+105del
ENST00000579047.5:c.645+83_645+105del	ENSP00000471369.1:n.645+83_645+105del
ENST00000579345.5:n.351+83_351+105del
ENST00000580878.1:n.488+83_488+105del
ENST00000584288.5:c.*445+83_*445+105del	ENSP00000462469.1:n.*445+83_*445+105del
NM_001243027.2:c.645+83_645+105del	NP_001229956.1:n.645+83_645+105del
NM_001243028.2:c.645+83_645+105del	NP_001229957.1:n.645+83_645+105del
NM_001626.5:c.831+83_831+105del	NP_001617.1:n.831+83_831+105del
XM_011526614.1:c.831+83_831+105del	XP_011524916.1:n.831+83_831+105del
XM_011526615.1:c.831+83_831+105del	XP_011524917.1:n.831+83_831+105del
XM_011526616.1:c.831+83_831+105del	XP_011524918.1:n.831+83_831+105del
XM_011526617.1:c.831+83_831+105del	XP_011524919.1:n.831+83_831+105del
XM_011526618.1:c.831+83_831+105del	XP_011524920.1:n.831+83_831+105del
XM_011526619.1:c.831+83_831+105del	XP_011524921.1:n.831+83_831+105del
XM_011526620.1:c.831+83_831+105del	XP_011524922.1:n.831+83_831+105del
XM_011526621.1:c.831+83_831+105del	XP_011524923.1:n.831+83_831+105del
XM_011526622.1:c.831+83_831+105del	XP_011524924.1:n.831+83_831+105del
NM_001330511.1:c.831+83_831+105del	NP_001317440.1:n.831+83_831+105del
XM_011526622.2:c.831+83_831+105del	XP_011524924.1:n.831+83_831+105del
XM_017026470.2:c.831+83_831+105del	XP_016881959.1:n.831+83_831+105del
XM_024451416.1:c.831+83_831+105del	XP_024307184.1:n.831+83_831+105del
XM_024451417.1:c.831+83_831+105del	XP_024307185.1:n.831+83_831+105del
NM_001626.6:c.831+83_831+105del MANE Select	NP_001617.1:n.831+83_831+105del
NM_001243027.3:c.645+83_645+105del	NP_001229956.1:n.645+83_645+105del
NM_001243028.3:c.645+83_645+105del	NP_001229957.1:n.645+83_645+105del