Canonical Allele Identifier: CA402954244

Gene: STK11

Linked Data

• gnomAD v4: 19-1226633-T-C
• MyVariant Identifiers: chr19:g.1226632T>C (hg19) ; chr19:g.1226633T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226633T>C , CM000681.2:g.1226633T>C	GRCh38
NC_000019.9:g.1226632T>C , CM000681.1:g.1226632T>C	GRCh37
NC_000019.8:g.1177632T>C	NCBI36
NG_007460.2:g.42227T>C , LRG_319:g.42227T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.*2889T>C	ENSP00000490268.2:n.*2889T>C
ENST00000585748.3:c.916T>C	ENSP00000477641.2:p.Cys306Arg
ENST00000585851.2:c.1114T>C	ENSP00000467912.2:p.Cys372Arg
ENST00000326873.12:c.1288T>C MANE Select	ENSP00000324856.6:p.Cys430Arg
ENST00000326873.11:c.1288T>C	ENSP00000324856.6:p.Cys430Arg
ENST00000585465.2:n.3021T>C
ENST00000586243.5:c.1285T>C	ENSP00000467240.2:p.Cys429Arg
ENST00000589152.5:n.1986T>C
NM_000455.4:c.1288T>C , LRG_319t1:c.1288T>C	NP_000446.1:p.Cys430Arg
XM_005259617.1:c.1283T>C	XP_005259674.1:p.Leu428Pro
XM_011528209.1:c.1061T>C	XP_011526511.1:p.Leu354Pro
XM_005259617.3:c.1283T>C	XP_005259674.1:p.Leu428Pro
XM_011528209.2:c.1061T>C	XP_011526511.1:p.Leu354Pro
XR_001753738.2:n.2094T>C
XR_001753740.2:n.2064T>C
NM_000455.5:c.1288T>C MANE Select	NP_000446.1:p.Cys430Arg