Canonical Allele Identifier: CA633110955

Gene: AKT2

Linked Data

• dbSNP Id: rs1177909068
• gnomAD v2: 19-40791192-CCGGCAGCGGCAGCGG-C
• gnomAD v3: 19-40285285-CCGGCAGCGGCAGCGG-C
• gnomAD v4: 19-40285285-CCGGCAGCGGCAGCGG-C
• MyVariant Identifiers: chr19:g.40791193_40791207del (hg19) ; chr19:g.40285286_40285300del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285290_40285304del , CM000681.2:g.40285290_40285304del	GRCh38
NC_000019.9:g.40791197_40791211del , CM000681.1:g.40791197_40791211del	GRCh37
NC_000019.8:g.45483037_45483051del	NCBI36
NG_012038.2:g.5059_5073del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.7:c.-204_-190del MANE Select	ENSP00000375892.2:n.-204_-190del
ENST00000391844.8:c.-250_-236del	ENSP00000375719.4:n.-250_-236del
ENST00000392038.6:c.-204_-190del	ENSP00000375892.2:n.-204_-190del
ENST00000424901.5:c.-204_-190del	ENSP00000399532.2:n.-204_-190del
ENST00000578123.5:c.-85+148_-85+162del	ENSP00000462022.1:n.-85+148_-85+162del
ENST00000579047.5:c.-260_-246del	ENSP00000471369.1:n.-260_-246del
ENST00000584288.5:c.-343_-329del	ENSP00000462469.1:n.-343_-329del
NM_001243027.2:c.-353_-339del	NP_001229956.1:n.-353_-339del
NM_001243028.2:c.-260_-246del	NP_001229957.1:n.-260_-246del
NM_001626.5:c.-204_-190del	NP_001617.1:n.-204_-190del
XM_011526620.1:c.-85+148_-85+162del	XP_011524922.1:n.-85+148_-85+162del
XM_011526622.1:c.-204_-190del	XP_011524924.1:n.-204_-190del
XM_011526622.2:c.-204_-190del	XP_011524924.1:n.-204_-190del
XM_024451417.1:c.-204_-190del	XP_024307185.1:n.-204_-190del
NM_001626.6:c.-204_-190del MANE Select	NP_001617.1:n.-204_-190del
NM_001243027.3:c.-353_-339del	NP_001229956.1:n.-353_-339del
NM_001243028.3:c.-260_-246del	NP_001229957.1:n.-260_-246del