Canonical Allele Identifier: CA2582592151

Gene: STK11

Linked Data

• gnomAD v4: 19-1219453-G-GGGGCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219456_1219457insCCCGGG , CM000681.2:g.1219456_1219457insCCCGGG	GRCh38
NC_000019.9:g.1219455_1219456insCCCGGG , CM000681.1:g.1219455_1219456insCCCGGG	GRCh37
NC_000019.8:g.1170455_1170456insCCCGGG	NCBI36
NG_007460.2:g.35050_35051insCCCGGG , LRG_319:g.35050_35051insCCCGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.464+43_464+44insCCCGGG	ENSP00000490268.2:n.464+43_464+44insCCCGGG
ENST00000585748.3:c.92+43_92+44insCCCGGG	ENSP00000477641.2:n.92+43_92+44insCCCGGG
ENST00000585851.2:c.291-917_291-916insCCCGGG	ENSP00000467912.2:n.291-917_291-916insCCCGGG
ENST00000326873.12:c.464+43_464+44insCCCGGG MANE Select	ENSP00000324856.6:n.464+43_464+44insCCCGGG
ENST00000652231.1:c.464+43_464+44insCCCGGG	ENSP00000498804.1:n.464+43_464+44insCCCGGG
ENST00000326873.11:c.464+43_464+44insCCCGGG	ENSP00000324856.6:n.464+43_464+44insCCCGGG
ENST00000585851.1:c.291-917_291-916insCCCGGG	ENSP00000467912.1:n.291-917_291-916insCCCGGG
ENST00000586243.5:c.464+43_464+44insCCCGGG	ENSP00000467240.2:n.464+43_464+44insCCCGGG
ENST00000586358.5:n.287+43_287+44insCCCGGG
ENST00000589152.5:n.554+43_554+44insCCCGGG
NM_000455.4:c.464+43_464+44insCCCGGG , LRG_319t1:c.464+43_464+44insCCCGGG	NP_000446.1:n.464+43_464+44insCCCGGG
XM_005259617.1:c.464+43_464+44insCCCGGG	XP_005259674.1:n.464+43_464+44insCCCGGG
XM_005259618.3:c.464+43_464+44insCCCGGG	XP_005259675.1:n.464+43_464+44insCCCGGG
XM_011528209.1:c.242+43_242+44insCCCGGG	XP_011526511.1:n.242+43_242+44insCCCGGG
XR_936204.1:n.1089+43_1089+44insCCCGGG
XM_005259617.3:c.464+43_464+44insCCCGGG	XP_005259674.1:n.464+43_464+44insCCCGGG
XM_011528209.2:c.242+43_242+44insCCCGGG	XP_011526511.1:n.242+43_242+44insCCCGGG
XR_001753738.2:n.1089+43_1089+44insCCCGGG
XR_001753739.1:n.1089+43_1089+44insCCCGGG
XR_001753740.2:n.1089+43_1089+44insCCCGGG
NM_000455.5:c.464+43_464+44insCCCGGG MANE Select	NP_000446.1:n.464+43_464+44insCCCGGG