Canonical Allele Identifier: CA2582592143

Gene: STK11

Linked Data

• dbSNP Id: rs2145422722
• gnomAD v4: 19-1219449-G-GGCCGGGA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219455_1219456insAGCCGGG , CM000681.2:g.1219455_1219456insAGCCGGG	GRCh38
NC_000019.9:g.1219454_1219455insAGCCGGG , CM000681.1:g.1219454_1219455insAGCCGGG	GRCh37
NC_000019.8:g.1170454_1170455insAGCCGGG	NCBI36
NG_007460.2:g.35049_35050insAGCCGGG , LRG_319:g.35049_35050insAGCCGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.464+42_464+43insAGCCGGG	ENSP00000490268.2:n.464+42_464+43insAGCCGGG
ENST00000585748.3:c.92+42_92+43insAGCCGGG	ENSP00000477641.2:n.92+42_92+43insAGCCGGG
ENST00000585851.2:c.291-918_291-917insAGCCGGG	ENSP00000467912.2:n.291-918_291-917insAGCCGGG
ENST00000326873.12:c.464+42_464+43insAGCCGGG MANE Select	ENSP00000324856.6:n.464+42_464+43insAGCCGGG
ENST00000652231.1:c.464+42_464+43insAGCCGGG	ENSP00000498804.1:n.464+42_464+43insAGCCGGG
ENST00000326873.11:c.464+42_464+43insAGCCGGG	ENSP00000324856.6:n.464+42_464+43insAGCCGGG
ENST00000585851.1:c.291-918_291-917insAGCCGGG	ENSP00000467912.1:n.291-918_291-917insAGCCGGG
ENST00000586243.5:c.464+42_464+43insAGCCGGG	ENSP00000467240.2:n.464+42_464+43insAGCCGGG
ENST00000586358.5:n.287+42_287+43insAGCCGGG
ENST00000589152.5:n.554+42_554+43insAGCCGGG
NM_000455.4:c.464+42_464+43insAGCCGGG , LRG_319t1:c.464+42_464+43insAGCCGGG	NP_000446.1:n.464+42_464+43insAGCCGGG
XM_005259617.1:c.464+42_464+43insAGCCGGG	XP_005259674.1:n.464+42_464+43insAGCCGGG
XM_005259618.3:c.464+42_464+43insAGCCGGG	XP_005259675.1:n.464+42_464+43insAGCCGGG
XM_011528209.1:c.242+42_242+43insAGCCGGG	XP_011526511.1:n.242+42_242+43insAGCCGGG
XR_936204.1:n.1089+42_1089+43insAGCCGGG
XM_005259617.3:c.464+42_464+43insAGCCGGG	XP_005259674.1:n.464+42_464+43insAGCCGGG
XM_011528209.2:c.242+42_242+43insAGCCGGG	XP_011526511.1:n.242+42_242+43insAGCCGGG
XR_001753738.2:n.1089+42_1089+43insAGCCGGG
XR_001753739.1:n.1089+42_1089+43insAGCCGGG
XR_001753740.2:n.1089+42_1089+43insAGCCGGG
NM_000455.5:c.464+42_464+43insAGCCGGG MANE Select	NP_000446.1:n.464+42_464+43insAGCCGGG