Canonical Allele Identifier: CA10581012

Gene: STK11

Linked Data

• ClinVar Variation Id: 233698
• ClinVar RCV Id: RCV000222875
• dbSNP Id: rs876660582
• MyVariant Identifiers: chr19:g.1221967_1221969del (hg19) ; chr19:g.1221968_1221970del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221968_1221970del , CM000681.2:g.1221968_1221970del	GRCh38
NC_000019.9:g.1221967_1221969del , CM000681.1:g.1221967_1221969del	GRCh37
NC_000019.8:g.1172967_1172969del	NCBI36
NG_007460.2:g.37562_37564del , LRG_319:g.37562_37564del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.882_884del	ENSP00000490268.2:p.Ala295del
ENST00000585748.3:c.510_512del	ENSP00000477641.2:p.Ala171del
ENST00000585851.2:c.708_710del	ENSP00000467912.2:p.Ala237del
ENST00000326873.12:c.882_884del MANE Select	ENSP00000324856.6:p.Ala295del
ENST00000652231.1:c.882_884del	ENSP00000498804.1:p.Ala295del
ENST00000326873.11:c.882_884del	ENSP00000324856.6:p.Ala295del
ENST00000586243.5:c.882_884del	ENSP00000467240.2:p.Ala295del
ENST00000589152.5:n.1580_1582del
ENST00000591133.2:n.853_855del
NM_000455.4:c.882_884del , LRG_319t1:c.882_884del	NP_000446.1:p.Ala295del
XM_005259617.1:c.882_884del	XP_005259674.1:p.Ala295del
XM_005259618.3:c.882_884del	XP_005259675.1:p.Ala295del
XM_011528209.1:c.660_662del	XP_011526511.1:p.Ala221del
XR_936204.1:n.1658_1660del
XM_005259617.3:c.882_884del	XP_005259674.1:p.Ala295del
XM_011528209.2:c.660_662del	XP_011526511.1:p.Ala221del
XR_001753738.2:n.1688_1690del
XR_001753739.1:n.1688_1690del
XR_001753740.2:n.1658_1660del
NM_000455.5:c.882_884del MANE Select	NP_000446.1:p.Ala295del