Canonical Allele Identifier: CA2582593320

Gene: STK11

Linked Data

• gnomAD v4: 19-1221503-AGGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221504_1221506del , CM000681.2:g.1221504_1221506del	GRCh38
NC_000019.9:g.1221503_1221505del , CM000681.1:g.1221503_1221505del	GRCh37
NC_000019.8:g.1172503_1172505del	NCBI36
NG_007460.2:g.37098_37100del , LRG_319:g.37098_37100del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.862+164_862+166del	ENSP00000490268.2:n.862+164_862+166del
ENST00000585748.3:c.490+164_490+166del	ENSP00000477641.2:n.490+164_490+166del
ENST00000585851.2:c.688+164_688+166del	ENSP00000467912.2:n.688+164_688+166del
ENST00000326873.12:c.862+164_862+166del MANE Select	ENSP00000324856.6:n.862+164_862+166del
ENST00000652231.1:c.862+164_862+166del	ENSP00000498804.1:n.862+164_862+166del
ENST00000326873.11:c.862+164_862+166del	ENSP00000324856.6:n.862+164_862+166del
ENST00000586243.5:c.862+164_862+166del	ENSP00000467240.2:n.862+164_862+166del
ENST00000586358.5:n.760+164_760+166del
ENST00000589152.5:n.1116_1118del
ENST00000591133.2:n.833+164_833+166del
NM_000455.4:c.862+164_862+166del , LRG_319t1:c.862+164_862+166del	NP_000446.1:n.862+164_862+166del
XM_005259617.1:c.862+164_862+166del	XP_005259674.1:n.862+164_862+166del
XM_005259618.3:c.862+164_862+166del	XP_005259675.1:n.862+164_862+166del
XM_011528209.1:c.640+164_640+166del	XP_011526511.1:n.640+164_640+166del
XR_936204.1:n.1487+164_1487+166del
XM_005259617.3:c.862+164_862+166del	XP_005259674.1:n.862+164_862+166del
XM_011528209.2:c.640+164_640+166del	XP_011526511.1:n.640+164_640+166del
XR_001753738.2:n.1488-162_1488-160del
XR_001753739.1:n.1488-162_1488-160del
XR_001753740.2:n.1487+164_1487+166del
NM_000455.5:c.862+164_862+166del MANE Select	NP_000446.1:n.862+164_862+166del