Canonical Allele Identifier: CA657476124

Gene: STK11

Linked Data

• dbSNP Id: rs2080668226
• gnomAD v3: 19-1206771-T-C
• gnomAD v4: 19-1206771-T-C
• COSMIC: COSN8256243

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206771T>C , CM000681.2:g.1206771T>C	GRCh38
NC_000019.9:g.1206770T>C , CM000681.1:g.1206770T>C	GRCh37
NC_000019.8:g.1157770T>C	NCBI36
NG_007460.2:g.22365T>C , LRG_319:g.22365T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.-143T>C	ENSP00000490268.2:n.-143T>C
ENST00000585748.3:c.-82-11646T>C	ENSP00000477641.2:n.-82-11646T>C
ENST00000326873.12:c.-143T>C MANE Select	ENSP00000324856.6:n.-143T>C
ENST00000652231.1:c.-143T>C	ENSP00000498804.1:n.-143T>C
ENST00000326873.11:c.-143T>C	ENSP00000324856.6:n.-143T>C
ENST00000585748.2:c.-82-11646T>C	ENSP00000477641.1:n.-82-11646T>C
ENST00000586243.5:c.-143T>C	ENSP00000467240.2:n.-143T>C
NM_000455.4:c.-143T>C , LRG_319t1:c.-143T>C	NP_000446.1:n.-143T>C
XM_005259617.1:c.-143T>C	XP_005259674.1:n.-143T>C
XM_005259618.3:c.-143T>C	XP_005259675.1:n.-143T>C
XM_011528209.1:c.-496T>C	XP_011526511.1:n.-496T>C
XR_936204.1:n.483T>C
XM_005259617.3:c.-143T>C	XP_005259674.1:n.-143T>C
XM_011528209.2:c.-496T>C	XP_011526511.1:n.-496T>C
XR_001753738.2:n.483T>C
XR_001753739.1:n.483T>C
XR_001753740.2:n.483T>C
NM_000455.5:c.-143T>C MANE Select	NP_000446.1:n.-143T>C