Canonical Allele Identifier: CA304016885

Gene: STK11

Linked Data

• dbSNP Id: rs760910801
• gnomAD v2: 19-1207266-T-TA
• gnomAD v3: 19-1207267-T-TA
• gnomAD v4: 19-1207267-T-TA
• MyVariant Identifiers: chr19:g.1207266_1207267insA (hg19) ; chr19:g.1207267_1207268insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207267_1207268insA , CM000681.2:g.1207267_1207268insA	GRCh38
NC_000019.9:g.1207266_1207267insA , CM000681.1:g.1207266_1207267insA	GRCh37
NC_000019.8:g.1158266_1158267insA	NCBI36
NG_007460.2:g.22861_22862insA , LRG_319:g.22861_22862insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.290+64_290+65insA	ENSP00000490268.2:n.290+64_290+65insA
ENST00000585748.3:c.-82-11150_-82-11149insA	ENSP00000477641.2:n.-82-11150_-82-11149insA
ENST00000585851.2:c.290+64_290+65insA	ENSP00000467912.2:n.290+64_290+65insA
ENST00000326873.12:c.290+64_290+65insA MANE Select	ENSP00000324856.6:n.290+64_290+65insA
ENST00000652231.1:c.290+64_290+65insA	ENSP00000498804.1:n.290+64_290+65insA
ENST00000326873.11:c.290+64_290+65insA	ENSP00000324856.6:n.290+64_290+65insA
ENST00000585748.2:c.-82-11150_-82-11149insA	ENSP00000477641.1:n.-82-11150_-82-11149insA
ENST00000585851.1:c.290+64_290+65insA	ENSP00000467912.1:n.290+64_290+65insA
ENST00000586243.5:c.290+64_290+65insA	ENSP00000467240.2:n.290+64_290+65insA
ENST00000586358.5:n.113+64_113+65insA
ENST00000589152.5:n.380+64_380+65insA
ENST00000593219.5:c.290+64_290+65insA	ENSP00000466610.1:n.290+64_290+65insA
NM_000455.4:c.290+64_290+65insA , LRG_319t1:c.290+64_290+65insA	NP_000446.1:n.290+64_290+65insA
XM_005259617.1:c.290+64_290+65insA	XP_005259674.1:n.290+64_290+65insA
XM_005259618.3:c.290+64_290+65insA	XP_005259675.1:n.290+64_290+65insA
XM_011528209.1:c.-64+64_-64+65insA	XP_011526511.1:n.-64+64_-64+65insA
XR_936204.1:n.915+64_915+65insA
XM_005259617.3:c.290+64_290+65insA	XP_005259674.1:n.290+64_290+65insA
XM_011528209.2:c.-64+64_-64+65insA	XP_011526511.1:n.-64+64_-64+65insA
XR_001753738.2:n.915+64_915+65insA
XR_001753739.1:n.915+64_915+65insA
XR_001753740.2:n.915+64_915+65insA
NM_000455.5:c.290+64_290+65insA MANE Select	NP_000446.1:n.290+64_290+65insA