Canonical Allele Identifier: CA2582592025

Gene: STK11

Linked Data

• gnomAD v4: 19-1219259-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219264del , CM000681.2:g.1219264del	GRCh38
NC_000019.9:g.1219263del , CM000681.1:g.1219263del	GRCh37
NC_000019.8:g.1170263del	NCBI36
NG_007460.2:g.34858del , LRG_319:g.34858del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.375-60del	ENSP00000490268.2:n.375-60del
ENST00000585748.3:c.3-60del	ENSP00000477641.2:n.3-60del
ENST00000585851.2:c.291-1109del	ENSP00000467912.2:n.291-1109del
ENST00000326873.12:c.375-60del MANE Select	ENSP00000324856.6:n.375-60del
ENST00000652231.1:c.375-60del	ENSP00000498804.1:n.375-60del
ENST00000326873.11:c.375-60del	ENSP00000324856.6:n.375-60del
ENST00000585748.2:c.3-60del	ENSP00000477641.1:n.3-60del
ENST00000585851.1:c.291-1109del	ENSP00000467912.1:n.291-1109del
ENST00000586243.5:c.375-60del	ENSP00000467240.2:n.375-60del
ENST00000586358.5:n.198-60del
ENST00000589152.5:n.465-60del
ENST00000593219.5:c.*200-60del	ENSP00000466610.1:n.*200-60del
NM_000455.4:c.375-60del , LRG_319t1:c.375-60del	NP_000446.1:n.375-60del
XM_005259617.1:c.375-60del	XP_005259674.1:n.375-60del
XM_005259618.3:c.375-60del	XP_005259675.1:n.375-60del
XM_011528209.1:c.153-60del	XP_011526511.1:n.153-60del
XR_936204.1:n.1000-60del
XM_005259617.3:c.375-60del	XP_005259674.1:n.375-60del
XM_011528209.2:c.153-60del	XP_011526511.1:n.153-60del
XR_001753738.2:n.1000-60del
XR_001753739.1:n.1000-60del
XR_001753740.2:n.1000-60del
NM_000455.5:c.375-60del MANE Select	NP_000446.1:n.375-60del