Canonical Allele Identifier: CA882232861

Gene: AKT2

Linked Data

• dbSNP Id: rs1424411652
• MyVariant Identifiers: chr19:g.40791258_40791271del (hg19) ; chr19:g.40285351_40285364del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285357_40285370del , CM000681.2:g.40285357_40285370del	GRCh38
NC_000019.9:g.40791264_40791277del , CM000681.1:g.40791264_40791277del	GRCh37
NC_000019.8:g.45483104_45483117del	NCBI36
NG_012038.2:g.4995_5008del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391844.8:c.-314_-301del	ENSP00000375719.4:n.-314_-301del
ENST00000392038.6:c.-268_-255del	ENSP00000375892.2:n.-268_-255del
ENST00000424901.5:c.-268_-255del	ENSP00000399532.2:n.-268_-255del
ENST00000578123.5:c.-85+84_-85+97del	ENSP00000462022.1:n.-85+84_-85+97del
NM_001243027.2:c.-417_-404del	NP_001229956.1:n.-417_-404del
NM_001243028.2:c.-324_-311del	NP_001229957.1:n.-324_-311del
NM_001626.5:c.-268_-255del	NP_001617.1:n.-268_-255del
XM_011526620.1:c.-85+84_-85+97del	XP_011524922.1:n.-85+84_-85+97del