Canonical Allele Identifier: CA2573155753

Gene: STK11

Linked Data

• ClinVar Variation Id: 1584875
• ClinVar RCV Id: RCV002102913
• dbSNP Id: rs2145420922
• gnomAD v4: 19-1218517-TGGGACC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218519_1218524del , CM000681.2:g.1218519_1218524del	GRCh38
NC_000019.9:g.1218518_1218523del , CM000681.1:g.1218518_1218523del	GRCh37
NC_000019.8:g.1169518_1169523del	NCBI36
NG_007460.2:g.34113_34118del , LRG_319:g.34113_34118del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.374+19_374+24del	ENSP00000490268.2:n.374+19_374+24del
ENST00000585748.3:c.2+19_2+24del	ENSP00000477641.2:n.2+19_2+24del
ENST00000585851.2:c.291-1854_291-1849del	ENSP00000467912.2:n.291-1854_291-1849del
ENST00000326873.12:c.374+19_374+24del MANE Select	ENSP00000324856.6:n.374+19_374+24del
ENST00000652231.1:c.374+19_374+24del	ENSP00000498804.1:n.374+19_374+24del
ENST00000326873.11:c.374+19_374+24del	ENSP00000324856.6:n.374+19_374+24del
ENST00000585748.2:c.2+19_2+24del	ENSP00000477641.1:n.2+19_2+24del
ENST00000585851.1:c.291-1854_291-1849del	ENSP00000467912.1:n.291-1854_291-1849del
ENST00000586243.5:c.374+19_374+24del	ENSP00000467240.2:n.374+19_374+24del
ENST00000586358.5:n.197+19_197+24del
ENST00000589152.5:n.464+19_464+24del
ENST00000593219.5:c.*199+19_*199+24del	ENSP00000466610.1:n.*199+19_*199+24del
NM_000455.4:c.374+19_374+24del , LRG_319t1:c.374+19_374+24del	NP_000446.1:n.374+19_374+24del
XM_005259617.1:c.374+19_374+24del	XP_005259674.1:n.374+19_374+24del
XM_005259618.3:c.374+19_374+24del	XP_005259675.1:n.374+19_374+24del
XM_011528209.1:c.152+19_152+24del	XP_011526511.1:n.152+19_152+24del
XR_936204.1:n.999+19_999+24del
XM_005259617.3:c.374+19_374+24del	XP_005259674.1:n.374+19_374+24del
XM_011528209.2:c.152+19_152+24del	XP_011526511.1:n.152+19_152+24del
XR_001753738.2:n.999+19_999+24del
XR_001753739.1:n.999+19_999+24del
XR_001753740.2:n.999+19_999+24del
NM_000455.5:c.374+19_374+24del MANE Select	NP_000446.1:n.374+19_374+24del