Canonical Allele Identifier: CA2735564675

Gene: STK11

Linked Data

• dbSNP Id: rs2145435730

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226438G>C , CM000681.2:g.1226438G>C	GRCh38
NC_000019.9:g.1226437G>C , CM000681.1:g.1226437G>C	GRCh37
NC_000019.8:g.1177437G>C	NCBI36
NG_007460.2:g.42032G>C , LRG_319:g.42032G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2694G>C	ENSP00000490268.2:n.*2694G>C
ENST00000585748.3:c.737-16G>C	ENSP00000477641.2:n.737-16G>C
ENST00000585851.2:c.935-16G>C	ENSP00000467912.2:n.935-16G>C
ENST00000326873.12:c.1109-16G>C MANE Select	ENSP00000324856.6:n.1109-16G>C
ENST00000326873.11:c.1109-16G>C	ENSP00000324856.6:n.1109-16G>C
ENST00000585465.2:n.2826G>C
ENST00000586243.5:c.1109-16G>C	ENSP00000467240.2:n.1109-16G>C
ENST00000589152.5:n.1807-16G>C
NM_000455.4:c.1109-16G>C , LRG_319t1:c.1109-16G>C	NP_000446.1:n.1109-16G>C
XM_005259617.1:c.1109-21G>C	XP_005259674.1:n.1109-21G>C
XM_011528209.1:c.887-21G>C	XP_011526511.1:n.887-21G>C
XM_005259617.3:c.1109-21G>C	XP_005259674.1:n.1109-21G>C
XM_011528209.2:c.887-21G>C	XP_011526511.1:n.887-21G>C
XR_001753738.2:n.1915-16G>C
XR_001753740.2:n.1885-16G>C
NM_000455.5:c.1109-16G>C MANE Select	NP_000446.1:n.1109-16G>C