Canonical Allele Identifier: CA2582593220

Gene: STK11

Linked Data

• gnomAD v4: 19-1221406-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221411dup , CM000681.2:g.1221411dup	GRCh38
NC_000019.9:g.1221410dup , CM000681.1:g.1221410dup	GRCh37
NC_000019.8:g.1172410dup	NCBI36
NG_007460.2:g.37005dup , LRG_319:g.37005dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.862+71dup	ENSP00000490268.2:n.862+71dup
ENST00000585748.3:c.490+71dup	ENSP00000477641.2:n.490+71dup
ENST00000585851.2:c.688+71dup	ENSP00000467912.2:n.688+71dup
ENST00000326873.12:c.862+71dup MANE Select	ENSP00000324856.6:n.862+71dup
ENST00000652231.1:c.862+71dup	ENSP00000498804.1:n.862+71dup
ENST00000326873.11:c.862+71dup	ENSP00000324856.6:n.862+71dup
ENST00000586243.5:c.862+71dup	ENSP00000467240.2:n.862+71dup
ENST00000586358.5:n.760+71dup
ENST00000589152.5:n.1023dup
ENST00000591133.2:n.833+71dup
NM_000455.4:c.862+71dup , LRG_319t1:c.862+71dup	NP_000446.1:n.862+71dup
XM_005259617.1:c.862+71dup	XP_005259674.1:n.862+71dup
XM_005259618.3:c.862+71dup	XP_005259675.1:n.862+71dup
XM_011528209.1:c.640+71dup	XP_011526511.1:n.640+71dup
XR_936204.1:n.1487+71dup
XM_005259617.3:c.862+71dup	XP_005259674.1:n.862+71dup
XM_011528209.2:c.640+71dup	XP_011526511.1:n.640+71dup
XR_001753738.2:n.1487+71dup
XR_001753739.1:n.1487+71dup
XR_001753740.2:n.1487+71dup
NM_000455.5:c.862+71dup MANE Select	NP_000446.1:n.862+71dup