Canonical Allele Identifier: CA2573155839

Gene: STK11

Linked Data

• ClinVar Variation Id: 1692440
• ClinVar RCV Id: RCV002257205
• dbSNP Id: rs876661012

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207092_1207093insAA , CM000681.2:g.1207092_1207093insAA	GRCh38
NC_000019.9:g.1207091_1207092insAA , CM000681.1:g.1207091_1207092insAA	GRCh37
NC_000019.8:g.1158091_1158092insAA	NCBI36
NG_007460.2:g.22686_22687insAA , LRG_319:g.22686_22687insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.179_180insAA	ENSP00000490268.2:p.Tyr60Ter
ENST00000585748.3:c.-82-11325_-82-11324insAA	ENSP00000477641.2:n.-82-11325_-82-11324insAA
ENST00000585851.2:c.179_180insAA	ENSP00000467912.2:p.Tyr60Ter
ENST00000326873.12:c.179_180insAA MANE Select	ENSP00000324856.6:p.Tyr60Ter
ENST00000652231.1:c.179_180insAA	ENSP00000498804.1:p.Tyr60Ter
ENST00000326873.11:c.179_180insAA	ENSP00000324856.6:p.Tyr60Ter
ENST00000585748.2:c.-82-11325_-82-11324insAA	ENSP00000477641.1:n.-82-11325_-82-11324insAA
ENST00000585851.1:c.179_180insAA	ENSP00000467912.1:p.Tyr60Ter
ENST00000586243.5:c.179_180insAA	ENSP00000467240.2:p.Tyr60Ter
ENST00000586358.5:n.2_3insAA
ENST00000589152.5:n.269_270insAA
ENST00000593219.5:c.179_180insAA	ENSP00000466610.1:p.Tyr60Ter
NM_000455.4:c.179_180insAA , LRG_319t1:c.179_180insAA	NP_000446.1:p.Tyr60Ter
XM_005259617.1:c.179_180insAA	XP_005259674.1:p.Tyr60Ter
XM_005259618.3:c.179_180insAA	XP_005259675.1:p.Tyr60Ter
XM_011528209.1:c.-175_-174insAA	XP_011526511.1:n.-175_-174insAA
XR_936204.1:n.804_805insAA
XM_005259617.3:c.179_180insAA	XP_005259674.1:p.Tyr60Ter
XM_011528209.2:c.-175_-174insAA	XP_011526511.1:n.-175_-174insAA
XR_001753738.2:n.804_805insAA
XR_001753739.1:n.804_805insAA
XR_001753740.2:n.804_805insAA
NM_000455.5:c.179_180insAA MANE Select	NP_000446.1:p.Tyr60Ter