Canonical Allele Identifier: CA645604088
Gene: STK11 HGNC NCBI

Linked Data

COSMIC: COSM27347

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1221213_1221340del , CM000681.2:g.1221213_1221340del GRCh38
NC_000019.9:g.1221212_1221339del , CM000681.1:g.1221212_1221339del GRCh37
NC_000019.8:g.1172212_1172339del NCBI36
NG_007460.2:g.36807_36934del , LRG_319:g.36807_36934del

Transcript Alleles

HGVS Amino-acid change
ENST00000585465.3:c.735_862del
ENST00000585748.3:c.363_490del
ENST00000585851.2:c.561_688del
ENST00000326873.12:c.735_862del
ENST00000652231.1:c.735_862del
ENST00000326873.11:c.735_862del
ENST00000586243.5:c.735_862del
ENST00000586358.5:n.633_760del
ENST00000589152.5:n.825_952del
ENST00000591133.2:n.706_833del
NM_000455.4:c.735_862del , LRG_319t1:c.735_862del
XM_005259617.1:c.735_862del
XM_005259618.3:c.735_862del
XM_011528209.1:c.513_640del
XR_936204.1:n.1360_1487del
XM_005259617.3:c.735_862del
XM_011528209.2:c.513_640del
XR_001753738.2:n.1360_1487del
XR_001753739.1:n.1360_1487del
XR_001753740.2:n.1360_1487del
NM_000455.5:c.735_862del