Canonical Allele Identifier: CA645369774

Gene: STK11

Linked Data

• ClinVar Variation Id: 428748
• ClinVar RCV Id: RCV000492248 ; RCV003507283
• dbSNP Id: rs1131690916
• COSMIC: COSM51519
• MyVariant Identifiers: chr19:g.1207063_1207074del (hg19) ; chr19:g.1207064_1207075del (hg38)
• PubMed: PMID:19892943 ; PMID:23415580

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207064_1207075del , CM000681.2:g.1207064_1207075del	GRCh38
NC_000019.9:g.1207063_1207074del , CM000681.1:g.1207063_1207074del	GRCh37
NC_000019.8:g.1158063_1158074del	NCBI36
NG_007460.2:g.22658_22669del , LRG_319:g.22658_22669del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.151_162del	ENSP00000490268.2:p.Met51_Leu54del
ENST00000585748.3:c.-82-11353_-82-11342del	ENSP00000477641.2:n.-82-11353_-82-11342del
ENST00000585851.2:c.151_162del	ENSP00000467912.2:p.Met51_Leu54del
ENST00000326873.12:c.151_162del MANE Select	ENSP00000324856.6:p.Met51_Leu54del
ENST00000652231.1:c.151_162del	ENSP00000498804.1:p.Met51_Leu54del
ENST00000326873.11:c.151_162del	ENSP00000324856.6:p.Met51_Leu54del
ENST00000585748.2:c.-82-11353_-82-11342del	ENSP00000477641.1:n.-82-11353_-82-11342del
ENST00000585851.1:c.151_162del	ENSP00000467912.1:p.Met51_Leu54del
ENST00000586243.5:c.151_162del	ENSP00000467240.2:p.Met51_Leu54del
ENST00000589152.5:n.241_252del
ENST00000593219.5:c.151_162del	ENSP00000466610.1:p.Met51_Leu54del
NM_000455.4:c.151_162del , LRG_319t1:c.151_162del	NP_000446.1:p.Met51_Leu54del
XM_005259617.1:c.151_162del	XP_005259674.1:p.Met51_Leu54del
XM_005259618.3:c.151_162del	XP_005259675.1:p.Met51_Leu54del
XM_011528209.1:c.-203_-192del	XP_011526511.1:n.-203_-192del
XR_936204.1:n.776_787del
XM_005259617.3:c.151_162del	XP_005259674.1:p.Met51_Leu54del
XM_011528209.2:c.-203_-192del	XP_011526511.1:n.-203_-192del
XR_001753738.2:n.776_787del
XR_001753739.1:n.776_787del
XR_001753740.2:n.776_787del
NM_000455.5:c.151_162del MANE Select	NP_000446.1:p.Met51_Leu54del