Canonical Allele Identifier: CA2499225350

Gene: STK11

Linked Data

• ClinVar Variation Id: 1050750
• ClinVar RCV Id: RCV001358560

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206912_1208216del , CM000681.2:g.1206912_1208216del	GRCh38
NC_000019.9:g.1206911_1208215del , CM000681.1:g.1206911_1208215del	GRCh37
NC_000019.8:g.1157911_1159215del	NCBI36
NG_007460.2:g.22506_23810del , LRG_319:g.22506_23810del

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.-2_290+1013del
ENST00000585748.3:c.-82-11505_-82-10201del	ENSP00000477641.2:n.-82-11505_-82-10201de...
ENST00000585851.2:c.-2_290+1013del
ENST00000326873.12:c.-2_290+1013del
ENST00000652231.1:c.-2_290+1013del
ENST00000326873.11:c.-2_290+1013del
ENST00000585748.2:c.-82-11505_-82-10201del	ENSP00000477641.1:n.-82-11505_-82-10201de...
ENST00000585851.1:c.-2_290+1013del
ENST00000586243.5:c.-2_290+1013del
ENST00000589152.5:n.89_380+1013del
ENST00000593219.5:c.-2_290+1013del
NM_000455.4:c.-2_290+1013del , LRG_319t1:c.-2_290+1013del
XM_005259617.1:c.-2_290+1013del
XM_005259618.3:c.-2_290+1013del
XM_011528209.1:c.-355_-64+1013del
XR_936204.1:n.624_915+1013del
XM_005259617.3:c.-2_290+1013del
XM_011528209.2:c.-355_-64+1013del
XR_001753738.2:n.624_915+1013del
XR_001753739.1:n.624_915+1013del
XR_001753740.2:n.624_915+1013del
NM_000455.5:c.-2_290+1013del