Canonical Allele Identifier: CA304025212

Gene: STK11

Linked Data

• ClinVar Variation Id: 2431071
• ClinVar RCV Id: RCV003129604
• dbSNP Id: rs775348337
• gnomAD v2: 19-1219551-G-GT
• gnomAD v3: 19-1219552-G-GT
• gnomAD v4: 19-1219552-G-GT
• MyVariant Identifiers: chr19:g.1219551_1219552insT (hg19) ; chr19:g.1219552_1219553insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219553dup , CM000681.2:g.1219553dup	GRCh38
NC_000019.9:g.1219552dup , CM000681.1:g.1219552dup	GRCh37
NC_000019.8:g.1170552dup	NCBI36
NG_007460.2:g.35147dup , LRG_319:g.35147dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.464+140dup	ENSP00000490268.2:n.464+140dup
ENST00000585748.3:c.92+140dup	ENSP00000477641.2:n.92+140dup
ENST00000585851.2:c.291-820dup	ENSP00000467912.2:n.291-820dup
ENST00000326873.12:c.464+140dup MANE Select	ENSP00000324856.6:n.464+140dup
ENST00000652231.1:c.464+140dup	ENSP00000498804.1:n.464+140dup
ENST00000326873.11:c.464+140dup	ENSP00000324856.6:n.464+140dup
ENST00000585851.1:c.291-820dup	ENSP00000467912.1:n.291-820dup
ENST00000586243.5:c.464+140dup	ENSP00000467240.2:n.464+140dup
ENST00000586358.5:n.287+140dup
ENST00000589152.5:n.554+140dup
NM_000455.4:c.464+140dup , LRG_319t1:c.464+140dup	NP_000446.1:n.464+140dup
XM_005259617.1:c.464+140dup	XP_005259674.1:n.464+140dup
XM_005259618.3:c.464+140dup	XP_005259675.1:n.464+140dup
XM_011528209.1:c.242+140dup	XP_011526511.1:n.242+140dup
XR_936204.1:n.1089+140dup
XM_005259617.3:c.464+140dup	XP_005259674.1:n.464+140dup
XM_011528209.2:c.242+140dup	XP_011526511.1:n.242+140dup
XR_001753738.2:n.1089+140dup
XR_001753739.1:n.1089+140dup
XR_001753740.2:n.1089+140dup
NM_000455.5:c.464+140dup MANE Select	NP_000446.1:n.464+140dup