Canonical Allele Identifier: CA882232901

Gene: AKT2

Linked Data

• dbSNP Id: rs1404810521
• gnomAD v3: 19-40285364-TC-T
• gnomAD v4: 19-40285364-TC-T
• MyVariant Identifiers: chr19:g.40791272del (hg19) ; chr19:g.40285365del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285370del , CM000681.2:g.40285370del	GRCh38
NC_000019.9:g.40791277del , CM000681.1:g.40791277del	GRCh37
NC_000019.8:g.45483117del	NCBI36
NG_012038.2:g.4994del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391844.8:c.-315del	ENSP00000375719.4:n.-315del
ENST00000392038.6:c.-269del	ENSP00000375892.2:n.-269del
ENST00000424901.5:c.-269del	ENSP00000399532.2:n.-269del
ENST00000578123.5:c.-85+83del	ENSP00000462022.1:n.-85+83del
NM_001243027.2:c.-418del	NP_001229956.1:n.-418del
NM_001243028.2:c.-325del	NP_001229957.1:n.-325del
NM_001626.5:c.-269del	NP_001617.1:n.-269del
XM_011526620.1:c.-85+83del	XP_011524922.1:n.-85+83del