Canonical Allele Identifier: CA2499225339

Gene: STK11

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218415_1218591del , CM000681.2:g.1218415_1218591del	GRCh38
NC_000019.9:g.1218414_1218590del , CM000681.1:g.1218414_1218590del	GRCh37
NC_000019.8:g.1169414_1169590del	NCBI36
NG_007460.2:g.34009_34185del , LRG_319:g.34009_34185del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.291-2_374+91del
ENST00000585748.3:c.-82-2_2+91del
ENST00000585851.2:c.291-1958_291-1782del	ENSP00000467912.2:n.291-1958_291-1782del
ENST00000326873.12:c.291-2_374+91del
ENST00000652231.1:c.291-2_374+91del
ENST00000326873.11:c.291-2_374+91del
ENST00000585748.2:c.-82-2_2+91del
ENST00000585851.1:c.291-1958_291-1782del	ENSP00000467912.1:n.291-1958_291-1782del
ENST00000586243.5:c.291-2_374+91del
ENST00000586358.5:n.114-2_197+91del
ENST00000589152.5:n.381-2_464+91del
ENST00000593219.5:c.*116-2_*199+91del
NM_000455.4:c.291-2_374+91del , LRG_319t1:c.291-2_374+91del
XM_005259617.1:c.291-2_374+91del
XM_005259618.3:c.291-2_374+91del
XM_011528209.1:c.69-2_152+91del
XR_936204.1:n.916-2_999+91del
XM_005259617.3:c.291-2_374+91del
XM_011528209.2:c.69-2_152+91del
XR_001753738.2:n.916-2_999+91del
XR_001753739.1:n.916-2_999+91del
XR_001753740.2:n.916-2_999+91del
NM_000455.5:c.291-2_374+91del