Canonical Allele Identifier: CA2735571403

Gene: STK11

Linked Data

• dbSNP Id: rs2145422680

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219450_1219451insGCGGGGGCCGGGGG , CM000681.2:g.1219450_1219451insGCGGGGGCCGGGGG	GRCh38
NC_000019.9:g.1219449_1219450insGCGGGGGCCGGGGG , CM000681.1:g.1219449_1219450insGCGGGGGCCGGGGG	GRCh37
NC_000019.8:g.1170449_1170450insGCGGGGGCCGGGGG	NCBI36
NG_007460.2:g.35044_35045insGCGGGGGCCGGGGG , LRG_319:g.35044_35045insGCGGGGGCCGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.464+37_464+38insGCGGGGGCCGGGGG	ENSP00000490268.2:n.464+37_464+38insGCGGGGGCCGGGGG
ENST00000585748.3:c.92+37_92+38insGCGGGGGCCGGGGG	ENSP00000477641.2:n.92+37_92+38insGCGGGGGCCGGGGG
ENST00000585851.2:c.291-923_291-922insGCGGGGGCCGGGGG	ENSP00000467912.2:n.291-923_291-922insGCGGGGGCCGGGGG
ENST00000326873.12:c.464+37_464+38insGCGGGGGCCGGGGG MANE Select	ENSP00000324856.6:n.464+37_464+38insGCGGGGGCCGGGGG
ENST00000652231.1:c.464+37_464+38insGCGGGGGCCGGGGG	ENSP00000498804.1:n.464+37_464+38insGCGGGGGCCGGGGG
ENST00000326873.11:c.464+37_464+38insGCGGGGGCCGGGGG	ENSP00000324856.6:n.464+37_464+38insGCGGGGGCCGGGGG
ENST00000585851.1:c.291-923_291-922insGCGGGGGCCGGGGG	ENSP00000467912.1:n.291-923_291-922insGCGGGGGCCGGGGG
ENST00000586243.5:c.464+37_464+38insGCGGGGGCCGGGGG	ENSP00000467240.2:n.464+37_464+38insGCGGGGGCCGGGGG
ENST00000586358.5:n.287+37_287+38insGCGGGGGCCGGGGG
ENST00000589152.5:n.554+37_554+38insGCGGGGGCCGGGGG
NM_000455.4:c.464+37_464+38insGCGGGGGCCGGGGG , LRG_319t1:c.464+37_464+38insGCGGGGGCCGGGGG	NP_000446.1:n.464+37_464+38insGCGGGGGCCGGGGG
XM_005259617.1:c.464+37_464+38insGCGGGGGCCGGGGG	XP_005259674.1:n.464+37_464+38insGCGGGGGCCGGGGG
XM_005259618.3:c.464+37_464+38insGCGGGGGCCGGGGG	XP_005259675.1:n.464+37_464+38insGCGGGGGCCGGGGG
XM_011528209.1:c.242+37_242+38insGCGGGGGCCGGGGG	XP_011526511.1:n.242+37_242+38insGCGGGGGCCGGGGG
XR_936204.1:n.1089+37_1089+38insGCGGGGGCCGGGGG
XM_005259617.3:c.464+37_464+38insGCGGGGGCCGGGGG	XP_005259674.1:n.464+37_464+38insGCGGGGGCCGGGGG
XM_011528209.2:c.242+37_242+38insGCGGGGGCCGGGGG	XP_011526511.1:n.242+37_242+38insGCGGGGGCCGGGGG
XR_001753738.2:n.1089+37_1089+38insGCGGGGGCCGGGGG
XR_001753739.1:n.1089+37_1089+38insGCGGGGGCCGGGGG
XR_001753740.2:n.1089+37_1089+38insGCGGGGGCCGGGGG
NM_000455.5:c.464+37_464+38insGCGGGGGCCGGGGG MANE Select	NP_000446.1:n.464+37_464+38insGCGGGGGCCGGGGG