Canonical Allele Identifier: CA9039455

Gene: STK11

Linked Data

• dbSNP Id: rs1555737868
• ExAC: 19:1219443 G / GCGTGGGGCGGGGGC
• gnomAD v4: 19-1219444-G-GCGTGGGGCGGGGGC
• MyVariant Identifiers: chr19:g.1219446_1219450delinsTGGGGCGGGGGCCGGGGGC (hg19) ; chr19:g.1219443_1219444insCGTGGGGCGGGGGC (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219446_1219447insTGGGGCGGGGGCCG , CM000681.2:g.1219446_1219447insTGGGGCGGGGGCCG	GRCh38
NC_000019.9:g.1219445_1219446insTGGGGCGGGGGCCG , CM000681.1:g.1219445_1219446insTGGGGCGGGGGCCG	GRCh37
NC_000019.8:g.1170445_1170446insTGGGGCGGGGGCCG	NCBI36
NG_007460.2:g.35040_35041insTGGGGCGGGGGCCG , LRG_319:g.35040_35041insTGGGGCGGGGGCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.464+33_464+34insTGGGGCGGGGGCCG	ENSP00000490268.2:n.464+33_464+34insTGGGGCGGGGGCCG
ENST00000585748.3:c.92+33_92+34insTGGGGCGGGGGCCG	ENSP00000477641.2:n.92+33_92+34insTGGGGCGGGGGCCG
ENST00000585851.2:c.291-927_291-926insTGGGGCGGGGGCCG	ENSP00000467912.2:n.291-927_291-926insTGGGGCGGGGGCCG
ENST00000326873.12:c.464+33_464+34insTGGGGCGGGGGCCG MANE Select	ENSP00000324856.6:n.464+33_464+34insTGGGGCGGGGGCCG
ENST00000652231.1:c.464+33_464+34insTGGGGCGGGGGCCG	ENSP00000498804.1:n.464+33_464+34insTGGGGCGGGGGCCG
ENST00000326873.11:c.464+33_464+34insTGGGGCGGGGGCCG	ENSP00000324856.6:n.464+33_464+34insTGGGGCGGGGGCCG
ENST00000585851.1:c.291-927_291-926insTGGGGCGGGGGCCG	ENSP00000467912.1:n.291-927_291-926insTGGGGCGGGGGCCG
ENST00000586243.5:c.464+33_464+34insTGGGGCGGGGGCCG	ENSP00000467240.2:n.464+33_464+34insTGGGGCGGGGGCCG
ENST00000586358.5:n.287+33_287+34insTGGGGCGGGGGCCG
ENST00000589152.5:n.554+33_554+34insTGGGGCGGGGGCCG
NM_000455.4:c.464+33_464+34insTGGGGCGGGGGCCG , LRG_319t1:c.464+33_464+34insTGGGGCGGGGGCCG	NP_000446.1:n.464+33_464+34insTGGGGCGGGGGCCG
XM_005259617.1:c.464+33_464+34insTGGGGCGGGGGCCG	XP_005259674.1:n.464+33_464+34insTGGGGCGGGGGCCG
XM_005259618.3:c.464+33_464+34insTGGGGCGGGGGCCG	XP_005259675.1:n.464+33_464+34insTGGGGCGGGGGCCG
XM_011528209.1:c.242+33_242+34insTGGGGCGGGGGCCG	XP_011526511.1:n.242+33_242+34insTGGGGCGGGGGCCG
XR_936204.1:n.1089+33_1089+34insTGGGGCGGGGGCCG
XM_005259617.3:c.464+33_464+34insTGGGGCGGGGGCCG	XP_005259674.1:n.464+33_464+34insTGGGGCGGGGGCCG
XM_011528209.2:c.242+33_242+34insTGGGGCGGGGGCCG	XP_011526511.1:n.242+33_242+34insTGGGGCGGGGGCCG
XR_001753738.2:n.1089+33_1089+34insTGGGGCGGGGGCCG
XR_001753739.1:n.1089+33_1089+34insTGGGGCGGGGGCCG
XR_001753740.2:n.1089+33_1089+34insTGGGGCGGGGGCCG
NM_000455.5:c.464+33_464+34insTGGGGCGGGGGCCG MANE Select	NP_000446.1:n.464+33_464+34insTGGGGCGGGGGCCG