Canonical Allele Identifier: CA2582592139

Gene: STK11

Linked Data

• gnomAD v4: 19-1219446-G-GGGGCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219449_1219450insCCCGGG , CM000681.2:g.1219449_1219450insCCCGGG	GRCh38
NC_000019.9:g.1219448_1219449insCCCGGG , CM000681.1:g.1219448_1219449insCCCGGG	GRCh37
NC_000019.8:g.1170448_1170449insCCCGGG	NCBI36
NG_007460.2:g.35043_35044insCCCGGG , LRG_319:g.35043_35044insCCCGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.464+36_464+37insCCCGGG	ENSP00000490268.2:n.464+36_464+37insCCCGGG
ENST00000585748.3:c.92+36_92+37insCCCGGG	ENSP00000477641.2:n.92+36_92+37insCCCGGG
ENST00000585851.2:c.291-924_291-923insCCCGGG	ENSP00000467912.2:n.291-924_291-923insCCCGGG
ENST00000326873.12:c.464+36_464+37insCCCGGG MANE Select	ENSP00000324856.6:n.464+36_464+37insCCCGGG
ENST00000652231.1:c.464+36_464+37insCCCGGG	ENSP00000498804.1:n.464+36_464+37insCCCGGG
ENST00000326873.11:c.464+36_464+37insCCCGGG	ENSP00000324856.6:n.464+36_464+37insCCCGGG
ENST00000585851.1:c.291-924_291-923insCCCGGG	ENSP00000467912.1:n.291-924_291-923insCCCGGG
ENST00000586243.5:c.464+36_464+37insCCCGGG	ENSP00000467240.2:n.464+36_464+37insCCCGGG
ENST00000586358.5:n.287+36_287+37insCCCGGG
ENST00000589152.5:n.554+36_554+37insCCCGGG
NM_000455.4:c.464+36_464+37insCCCGGG , LRG_319t1:c.464+36_464+37insCCCGGG	NP_000446.1:n.464+36_464+37insCCCGGG
XM_005259617.1:c.464+36_464+37insCCCGGG	XP_005259674.1:n.464+36_464+37insCCCGGG
XM_005259618.3:c.464+36_464+37insCCCGGG	XP_005259675.1:n.464+36_464+37insCCCGGG
XM_011528209.1:c.242+36_242+37insCCCGGG	XP_011526511.1:n.242+36_242+37insCCCGGG
XR_936204.1:n.1089+36_1089+37insCCCGGG
XM_005259617.3:c.464+36_464+37insCCCGGG	XP_005259674.1:n.464+36_464+37insCCCGGG
XM_011528209.2:c.242+36_242+37insCCCGGG	XP_011526511.1:n.242+36_242+37insCCCGGG
XR_001753738.2:n.1089+36_1089+37insCCCGGG
XR_001753739.1:n.1089+36_1089+37insCCCGGG
XR_001753740.2:n.1089+36_1089+37insCCCGGG
NM_000455.5:c.464+36_464+37insCCCGGG MANE Select	NP_000446.1:n.464+36_464+37insCCCGGG