Canonical Allele Identifier: CA1139666183

Gene: STK11

Linked Data

• ClinVar Variation Id: 934033
• ClinVar RCV Id: RCV001202362
• dbSNP Id: rs2080766077

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219416_1219881del , CM000681.2:g.1219416_1219881del	GRCh38
NC_000019.9:g.1219415_1219880del , CM000681.1:g.1219415_1219880del	GRCh37
NC_000019.8:g.1170415_1170880del	NCBI36
NG_007460.2:g.35010_35475del , LRG_319:g.35010_35475del

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.464+3_464+468del
ENST00000585748.3:c.92+3_92+468del
ENST00000585851.2:c.291-957_291-492del	ENSP00000467912.2:n.291-957_291-492del
ENST00000326873.12:c.464+3_464+468del
ENST00000652231.1:c.464+3_464+468del
ENST00000326873.11:c.464+3_464+468del
ENST00000585851.1:c.291-957_291-492del	ENSP00000467912.1:n.291-957_291-492del
ENST00000586243.5:c.464+3_464+468del
ENST00000586358.5:n.287+3_287+468del
ENST00000589152.5:n.554+3_554+468del
NM_000455.4:c.464+3_464+468del , LRG_319t1:c.464+3_464+468del
XM_005259617.1:c.464+3_464+468del
XM_005259618.3:c.464+3_464+468del
XM_011528209.1:c.242+3_242+468del
XR_936204.1:n.1089+3_1089+468del
XM_005259617.3:c.464+3_464+468del
XM_011528209.2:c.242+3_242+468del
XR_001753738.2:n.1089+3_1089+468del
XR_001753739.1:n.1089+3_1089+468del
XR_001753740.2:n.1089+3_1089+468del
NM_000455.5:c.464+3_464+468del