Canonical Allele Identifier: CA2580096021

Gene: STK11

Linked Data

• ClinVar Variation Id: 2004101
• ClinVar RCV Id: RCV002828178

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226438dup , CM000681.2:g.1226438dup	GRCh38
NC_000019.9:g.1226437dup , CM000681.1:g.1226437dup	GRCh37
NC_000019.8:g.1177437dup	NCBI36
NG_007460.2:g.42032dup , LRG_319:g.42032dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2694dup	ENSP00000490268.2:n.*2694dup
ENST00000585748.3:c.737-16dup	ENSP00000477641.2:n.737-16dup
ENST00000585851.2:c.935-16dup	ENSP00000467912.2:n.935-16dup
ENST00000326873.12:c.1109-16dup MANE Select	ENSP00000324856.6:n.1109-16dup
ENST00000326873.11:c.1109-16dup	ENSP00000324856.6:n.1109-16dup
ENST00000585465.2:n.2826dup
ENST00000586243.5:c.1109-16dup	ENSP00000467240.2:n.1109-16dup
ENST00000589152.5:n.1807-16dup
NM_000455.4:c.1109-16dup , LRG_319t1:c.1109-16dup	NP_000446.1:n.1109-16dup
XM_005259617.1:c.1109-21dup	XP_005259674.1:n.1109-21dup
XM_011528209.1:c.887-21dup	XP_011526511.1:n.887-21dup
XM_005259617.3:c.1109-21dup	XP_005259674.1:n.1109-21dup
XM_011528209.2:c.887-21dup	XP_011526511.1:n.887-21dup
XR_001753738.2:n.1915-16dup
XR_001753740.2:n.1885-16dup
NM_000455.5:c.1109-16dup MANE Select	NP_000446.1:n.1109-16dup