Canonical Allele Identifier: CA3260672624

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218407_1218510del , CM000681.2:g.1218407_1218510del	GRCh38
NC_000019.9:g.1218406_1218509del , CM000681.1:g.1218406_1218509del	GRCh37
NC_000019.8:g.1169406_1169509del	NCBI36
NG_007460.2:g.34001_34104del , LRG_319:g.34001_34104del

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.4:c.291-10_374+10del , LRG_319t1:c.291-10_374+10del
NM_000455.5:c.291-10_374+10del
ENST00000326873.11:c.291-10_374+10del
ENST00000326873.12:c.291-10_374+10del
ENST00000585465.3:c.291-10_374+10del
ENST00000585748.2:c.-82-10_2+10del
ENST00000585748.3:c.-82-10_2+10del
ENST00000585851.1:c.291-1966_291-1863del	ENSP00000467912.1:n.291-1966_291-1863del
ENST00000585851.2:c.291-1966_291-1863del	ENSP00000467912.2:n.291-1966_291-1863del
ENST00000586243.5:c.291-10_374+10del
ENST00000586358.5:n.114-10_197+10del
ENST00000589152.5:n.381-10_464+10del
ENST00000593219.5:c.*116-10_*199+10del
ENST00000652231.1:c.291-10_374+10del
XM_005259617.1:c.291-10_374+10del
XM_005259617.3:c.291-10_374+10del
XM_005259618.3:c.291-10_374+10del
XM_011528209.1:c.69-10_152+10del
XM_011528209.2:c.69-10_152+10del
XR_001753738.2:n.916-10_999+10del
XR_001753739.1:n.916-10_999+10del
XR_001753740.2:n.916-10_999+10del
XR_936204.1:n.916-10_999+10del