Canonical Allele Identifier: CA882232852

Gene: AKT2

Linked Data

• dbSNP Id: rs1165478099
• gnomAD v3: 19-40285349-G-GCC
• gnomAD v4: 19-40285349-G-GCC
• MyVariant Identifiers: chr19:g.40791256_40791257insCC (hg19) ; chr19:g.40285349_40285350insCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285356_40285357dup , CM000681.2:g.40285356_40285357dup	GRCh38
NC_000019.9:g.40791263_40791264dup , CM000681.1:g.40791263_40791264dup	GRCh37
NC_000019.8:g.45483103_45483104dup	NCBI36
NG_012038.2:g.5008_5009dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391844.8:c.-301_-300dup	ENSP00000375719.4:n.-301_-300dup
ENST00000392038.6:c.-255_-254dup	ENSP00000375892.2:n.-255_-254dup
ENST00000424901.5:c.-255_-254dup	ENSP00000399532.2:n.-255_-254dup
ENST00000578123.5:c.-85+97_-85+98dup	ENSP00000462022.1:n.-85+97_-85+98dup
NM_001243027.2:c.-404_-403dup	NP_001229956.1:n.-404_-403dup
NM_001243028.2:c.-311_-310dup	NP_001229957.1:n.-311_-310dup
NM_001626.5:c.-255_-254dup	NP_001617.1:n.-255_-254dup
XM_011526620.1:c.-85+97_-85+98dup	XP_011524922.1:n.-85+97_-85+98dup