Canonical Allele Identifier: CA2582592116

Gene: STK11

Linked Data

• gnomAD v4: 19-1219440-T-TGGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219444_1219445insGGGGGG , CM000681.2:g.1219444_1219445insGGGGGG	GRCh38
NC_000019.9:g.1219443_1219444insGGGGGG , CM000681.1:g.1219443_1219444insGGGGGG	GRCh37
NC_000019.8:g.1170443_1170444insGGGGGG	NCBI36
NG_007460.2:g.35038_35039insGGGGGG , LRG_319:g.35038_35039insGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.464+31_464+32insGGGGGG	ENSP00000490268.2:n.464+31_464+32insGGGGGG
ENST00000585748.3:c.92+31_92+32insGGGGGG	ENSP00000477641.2:n.92+31_92+32insGGGGGG
ENST00000585851.2:c.291-929_291-928insGGGGGG	ENSP00000467912.2:n.291-929_291-928insGGGGGG
ENST00000326873.12:c.464+31_464+32insGGGGGG MANE Select	ENSP00000324856.6:n.464+31_464+32insGGGGGG
ENST00000652231.1:c.464+31_464+32insGGGGGG	ENSP00000498804.1:n.464+31_464+32insGGGGGG
ENST00000326873.11:c.464+31_464+32insGGGGGG	ENSP00000324856.6:n.464+31_464+32insGGGGGG
ENST00000585851.1:c.291-929_291-928insGGGGGG	ENSP00000467912.1:n.291-929_291-928insGGGGGG
ENST00000586243.5:c.464+31_464+32insGGGGGG	ENSP00000467240.2:n.464+31_464+32insGGGGGG
ENST00000586358.5:n.287+31_287+32insGGGGGG
ENST00000589152.5:n.554+31_554+32insGGGGGG
NM_000455.4:c.464+31_464+32insGGGGGG , LRG_319t1:c.464+31_464+32insGGGGGG	NP_000446.1:n.464+31_464+32insGGGGGG
XM_005259617.1:c.464+31_464+32insGGGGGG	XP_005259674.1:n.464+31_464+32insGGGGGG
XM_005259618.3:c.464+31_464+32insGGGGGG	XP_005259675.1:n.464+31_464+32insGGGGGG
XM_011528209.1:c.242+31_242+32insGGGGGG	XP_011526511.1:n.242+31_242+32insGGGGGG
XR_936204.1:n.1089+31_1089+32insGGGGGG
XM_005259617.3:c.464+31_464+32insGGGGGG	XP_005259674.1:n.464+31_464+32insGGGGGG
XM_011528209.2:c.242+31_242+32insGGGGGG	XP_011526511.1:n.242+31_242+32insGGGGGG
XR_001753738.2:n.1089+31_1089+32insGGGGGG
XR_001753739.1:n.1089+31_1089+32insGGGGGG
XR_001753740.2:n.1089+31_1089+32insGGGGGG
NM_000455.5:c.464+31_464+32insGGGGGG MANE Select	NP_000446.1:n.464+31_464+32insGGGGGG