Canonical Allele Identifier: CA891843675

Gene: STK11

Linked Data

• ClinVar Variation Id: 568813
• ClinVar RCV Id: RCV000689283 ; RCV001016914
• dbSNP Id: rs1568690546
• MyVariant Identifiers: chr19:g.1207204_1207206del (hg19) ; chr19:g.1207205_1207207del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207205_1207207del , CM000681.2:g.1207205_1207207del	GRCh38
NC_000019.9:g.1207204_1207206del , CM000681.1:g.1207204_1207206del	GRCh37
NC_000019.8:g.1158204_1158206del	NCBI36
NG_007460.2:g.22799_22801del , LRG_319:g.22799_22801del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.290+2_290+4del	ENSP00000490268.2:n.290+2_290+4del
ENST00000585748.3:c.-82-11212_-82-11210del	ENSP00000477641.2:n.-82-11212_-82-11210del
ENST00000585851.2:c.290+2_290+4del	ENSP00000467912.2:n.290+2_290+4del
ENST00000326873.12:c.290+2_290+4del MANE Select	ENSP00000324856.6:n.290+2_290+4del
ENST00000652231.1:c.290+2_290+4del	ENSP00000498804.1:n.290+2_290+4del
ENST00000326873.11:c.290+2_290+4del	ENSP00000324856.6:n.290+2_290+4del
ENST00000585748.2:c.-82-11212_-82-11210del	ENSP00000477641.1:n.-82-11212_-82-11210del
ENST00000585851.1:c.290+2_290+4del	ENSP00000467912.1:n.290+2_290+4del
ENST00000586243.5:c.290+2_290+4del	ENSP00000467240.2:n.290+2_290+4del
ENST00000586358.5:n.113+2_113+4del
ENST00000589152.5:n.380+2_380+4del
ENST00000593219.5:c.290+2_290+4del	ENSP00000466610.1:n.290+2_290+4del
NM_000455.4:c.290+2_290+4del , LRG_319t1:c.290+2_290+4del	NP_000446.1:n.290+2_290+4del
XM_005259617.1:c.290+2_290+4del	XP_005259674.1:n.290+2_290+4del
XM_005259618.3:c.290+2_290+4del	XP_005259675.1:n.290+2_290+4del
XM_011528209.1:c.-64+2_-64+4del	XP_011526511.1:n.-64+2_-64+4del
XR_936204.1:n.915+2_915+4del
XM_005259617.3:c.290+2_290+4del	XP_005259674.1:n.290+2_290+4del
XM_011528209.2:c.-64+2_-64+4del	XP_011526511.1:n.-64+2_-64+4del
XR_001753738.2:n.915+2_915+4del
XR_001753739.1:n.915+2_915+4del
XR_001753740.2:n.915+2_915+4del
NM_000455.5:c.290+2_290+4del MANE Select	NP_000446.1:n.290+2_290+4del