Canonical Allele Identifier: CA645369772

Gene: STK11

Linked Data

• ClinVar Variation Id: 428766
• ClinVar RCV Id: RCV000492722
• dbSNP Id: rs1131690930
• MyVariant Identifiers: chr19:g.1207005dup (hg19) ; chr19:g.1207006dup (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1207006dup , CM000681.2:g.1207006dup	GRCh38
NC_000019.9:g.1207005dup , CM000681.1:g.1207005dup	GRCh37
NC_000019.8:g.1158005dup	NCBI36
NG_007460.2:g.22600dup , LRG_319:g.22600dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.93dup	ENSP00000490268.2:p.Thr32HisfsTer?
ENST00000585748.3:c.-82-11411dup	ENSP00000477641.2:n.-82-11411dup
ENST00000585851.2:c.93dup	ENSP00000467912.2:p.Thr32HisfsTer?
ENST00000326873.12:c.93dup MANE Select	ENSP00000324856.6:p.Thr32HisfsTer?
ENST00000652231.1:c.93dup	ENSP00000498804.1:p.Thr32HisfsTer?
ENST00000326873.11:c.93dup	ENSP00000324856.6:p.Thr32HisfsTer?
ENST00000585748.2:c.-82-11411dup	ENSP00000477641.1:n.-82-11411dup
ENST00000585851.1:c.93dup	ENSP00000467912.1:p.Thr32HisfsTer?
ENST00000586243.5:c.93dup	ENSP00000467240.2:p.Thr32HisfsTer?
ENST00000589152.5:n.183dup
ENST00000593219.5:c.93dup	ENSP00000466610.1:p.Thr32HisfsTer?
NM_000455.4:c.93dup , LRG_319t1:c.93dup	NP_000446.1:p.Thr32HisfsTer?
XM_005259617.1:c.93dup	XP_005259674.1:p.Thr32HisfsTer?
XM_005259618.3:c.93dup	XP_005259675.1:p.Thr32HisfsTer?
XM_011528209.1:c.-261dup	XP_011526511.1:n.-261dup
XR_936204.1:n.718dup
XM_005259617.3:c.93dup	XP_005259674.1:p.Thr32HisfsTer?
XM_011528209.2:c.-261dup	XP_011526511.1:n.-261dup
XR_001753738.2:n.718dup
XR_001753739.1:n.718dup
XR_001753740.2:n.718dup
NM_000455.5:c.93dup MANE Select	NP_000446.1:p.Thr32HisfsTer?