Canonical Allele Identifier: CA633110967
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs1165478099
gnomAD v2: 19-40791256-G-GC
gnomAD v3: 19-40285349-G-GC
gnomAD v4: 19-40285349-G-GC
MyVariant Identifiers: chr19:g.40791257_40791258insC (hg19) chr19:g.40791256_40791257insC (hg19) chr19:g.40285350_40285351insC (hg38) chr19:g.40285349_40285350insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285357dup , CM000681.2:g.40285357dup GRCh38
NC_000019.9:g.40791264dup , CM000681.1:g.40791264dup GRCh37
NC_000019.8:g.45483104dup NCBI36
NG_012038.2:g.5009dup

Transcript Alleles

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