Canonical Allele Identifier: CA402954324

Gene: STK11

Linked Data

• dbSNP Id: rs1333158922
• MyVariant Identifiers: chr19:g.1226645G>C (hg19) ; chr19:g.1226646G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226646G>C , CM000681.2:g.1226646G>C	GRCh38
NC_000019.9:g.1226645G>C , CM000681.1:g.1226645G>C	GRCh37
NC_000019.8:g.1177645G>C	NCBI36
NG_007460.2:g.42240G>C , LRG_319:g.42240G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2902G>C	ENSP00000490268.2:n.*2902G>C
ENST00000585748.3:c.929G>C	ENSP00000477641.2:p.Ter310Ser
ENST00000585851.2:c.1127G>C	ENSP00000467912.2:p.Ter376Ser
ENST00000326873.12:c.1301G>C MANE Select	ENSP00000324856.6:p.Ter434Ser
ENST00000326873.11:c.1301G>C	ENSP00000324856.6:p.Ter434Ser
ENST00000585465.2:n.3034G>C
ENST00000586243.5:c.1298G>C	ENSP00000467240.2:p.Ter433Ser
ENST00000589152.5:n.1999G>C
NM_000455.4:c.1301G>C , LRG_319t1:c.1301G>C	NP_000446.1:p.Ter434Ser
XM_005259617.1:c.1296G>C	XP_005259674.1:p.Val432=
XM_011528209.1:c.1074G>C	XP_011526511.1:p.Val358=
XM_005259617.3:c.1296G>C	XP_005259674.1:p.Val432=
XM_011528209.2:c.1074G>C	XP_011526511.1:p.Val358=
XR_001753738.2:n.2107G>C
XR_001753740.2:n.2077G>C
NM_000455.5:c.1301G>C MANE Select	NP_000446.1:p.Ter434Ser