Canonical Allele Identifier: CA2582591828

Gene: STK11

Linked Data

• gnomAD v4: 19-1218533-CCGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218534_1218536del , CM000681.2:g.1218534_1218536del	GRCh38
NC_000019.9:g.1218533_1218535del , CM000681.1:g.1218533_1218535del	GRCh37
NC_000019.8:g.1169533_1169535del	NCBI36
NG_007460.2:g.34128_34130del , LRG_319:g.34128_34130del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.374+34_374+36del	ENSP00000490268.2:n.374+34_374+36del
ENST00000585748.3:c.2+34_2+36del	ENSP00000477641.2:n.2+34_2+36del
ENST00000585851.2:c.291-1839_291-1837del	ENSP00000467912.2:n.291-1839_291-1837del
ENST00000326873.12:c.374+34_374+36del MANE Select	ENSP00000324856.6:n.374+34_374+36del
ENST00000652231.1:c.374+34_374+36del	ENSP00000498804.1:n.374+34_374+36del
ENST00000326873.11:c.374+34_374+36del	ENSP00000324856.6:n.374+34_374+36del
ENST00000585748.2:c.2+34_2+36del	ENSP00000477641.1:n.2+34_2+36del
ENST00000585851.1:c.291-1839_291-1837del	ENSP00000467912.1:n.291-1839_291-1837del
ENST00000586243.5:c.374+34_374+36del	ENSP00000467240.2:n.374+34_374+36del
ENST00000586358.5:n.197+34_197+36del
ENST00000589152.5:n.464+34_464+36del
ENST00000593219.5:c.*199+34_*199+36del	ENSP00000466610.1:n.*199+34_*199+36del
NM_000455.4:c.374+34_374+36del , LRG_319t1:c.374+34_374+36del	NP_000446.1:n.374+34_374+36del
XM_005259617.1:c.374+34_374+36del	XP_005259674.1:n.374+34_374+36del
XM_005259618.3:c.374+34_374+36del	XP_005259675.1:n.374+34_374+36del
XM_011528209.1:c.152+34_152+36del	XP_011526511.1:n.152+34_152+36del
XR_936204.1:n.999+34_999+36del
XM_005259617.3:c.374+34_374+36del	XP_005259674.1:n.374+34_374+36del
XM_011528209.2:c.152+34_152+36del	XP_011526511.1:n.152+34_152+36del
XR_001753738.2:n.999+34_999+36del
XR_001753739.1:n.999+34_999+36del
XR_001753740.2:n.999+34_999+36del
NM_000455.5:c.374+34_374+36del MANE Select	NP_000446.1:n.374+34_374+36del