Canonical Allele Identifier: CA504706283

Gene: STK11

Linked Data

• ClinVar Variation Id: 503650
• ClinVar RCV Id: RCV000598927 ; RCV000813229 ; RCV001178644
• dbSNP Id: rs1555735008
• COSMIC: COSM27322
• MyVariant Identifiers: chr19:g.1207092del (hg19) ; chr19:g.1207093del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207093del , CM000681.2:g.1207093del	GRCh38
NC_000019.9:g.1207092del , CM000681.1:g.1207092del	GRCh37
NC_000019.8:g.1158092del	NCBI36
NG_007460.2:g.22687del , LRG_319:g.22687del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.180del	ENSP00000490268.2:p.Tyr60Ter
ENST00000585748.3:c.-82-11324del	ENSP00000477641.2:n.-82-11324del
ENST00000585851.2:c.180del	ENSP00000467912.2:p.Tyr60Ter
ENST00000326873.12:c.180del MANE Select	ENSP00000324856.6:p.Tyr60Ter
ENST00000652231.1:c.180del	ENSP00000498804.1:p.Tyr60Ter
ENST00000326873.11:c.180del	ENSP00000324856.6:p.Tyr60Ter
ENST00000585748.2:c.-82-11324del	ENSP00000477641.1:n.-82-11324del
ENST00000585851.1:c.180del	ENSP00000467912.1:p.Tyr60Ter
ENST00000586243.5:c.180del	ENSP00000467240.2:p.Tyr60Ter
ENST00000586358.5:n.3del
ENST00000589152.5:n.270del
ENST00000593219.5:c.180del	ENSP00000466610.1:p.Tyr60Ter
NM_000455.4:c.180del , LRG_319t1:c.180del	NP_000446.1:p.Tyr60Ter
XM_005259617.1:c.180del	XP_005259674.1:p.Tyr60Ter
XM_005259618.3:c.180del	XP_005259675.1:p.Tyr60Ter
XM_011528209.1:c.-174del	XP_011526511.1:n.-174del
XR_936204.1:n.805del
XM_005259617.3:c.180del	XP_005259674.1:p.Tyr60Ter
XM_011528209.2:c.-174del	XP_011526511.1:n.-174del
XR_001753738.2:n.805del
XR_001753739.1:n.805del
XR_001753740.2:n.805del
NM_000455.5:c.180del MANE Select	NP_000446.1:p.Tyr60Ter