Canonical Allele Identifier: CA304026686

Gene: STK11

Linked Data

• dbSNP Id: rs751154109
• gnomAD v3: 19-1221127-CCT-C
• gnomAD v4: 19-1221127-CCT-C
• MyVariant Identifiers: chr19:g.1221127_1221128del (hg19) ; chr19:g.1221128_1221129del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221130_1221131del , CM000681.2:g.1221130_1221131del	GRCh38
NC_000019.9:g.1221129_1221130del , CM000681.1:g.1221129_1221130del	GRCh37
NC_000019.8:g.1172129_1172130del	NCBI36
NG_007460.2:g.36724_36725del , LRG_319:g.36724_36725del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.735-83_735-82del	ENSP00000490268.2:n.735-83_735-82del
ENST00000585748.3:c.363-83_363-82del	ENSP00000477641.2:n.363-83_363-82del
ENST00000585851.2:c.561-83_561-82del	ENSP00000467912.2:n.561-83_561-82del
ENST00000326873.12:c.735-83_735-82del MANE Select	ENSP00000324856.6:n.735-83_735-82del
ENST00000652231.1:c.735-83_735-82del	ENSP00000498804.1:n.735-83_735-82del
ENST00000326873.11:c.735-83_735-82del	ENSP00000324856.6:n.735-83_735-82del
ENST00000586243.5:c.735-83_735-82del	ENSP00000467240.2:n.735-83_735-82del
ENST00000586358.5:n.633-83_633-82del
ENST00000589152.5:n.825-83_825-82del
ENST00000591133.2:n.706-83_706-82del
NM_000455.4:c.735-83_735-82del , LRG_319t1:c.735-83_735-82del	NP_000446.1:n.735-83_735-82del
XM_005259617.1:c.735-83_735-82del	XP_005259674.1:n.735-83_735-82del
XM_005259618.3:c.735-83_735-82del	XP_005259675.1:n.735-83_735-82del
XM_011528209.1:c.513-83_513-82del	XP_011526511.1:n.513-83_513-82del
XR_936204.1:n.1360-83_1360-82del
XM_005259617.3:c.735-83_735-82del	XP_005259674.1:n.735-83_735-82del
XM_011528209.2:c.513-83_513-82del	XP_011526511.1:n.513-83_513-82del
XR_001753738.2:n.1360-83_1360-82del
XR_001753739.1:n.1360-83_1360-82del
XR_001753740.2:n.1360-83_1360-82del
NM_000455.5:c.735-83_735-82del MANE Select	NP_000446.1:n.735-83_735-82del