Canonical Allele Identifier: CA504707750

Gene: STK11

Linked Data

• ClinVar Variation Id: 485013
• ClinVar RCV Id: RCV000564037
• dbSNP Id: rs1555739204
• MyVariant Identifiers: chr19:g.1223041A>C (hg19) ; chr19:g.1223042A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223042A>C , CM000681.2:g.1223042A>C	GRCh38
NC_000019.9:g.1223041A>C , CM000681.1:g.1223041A>C	GRCh37
NC_000019.8:g.1174041A>C	NCBI36
NG_007460.2:g.38636A>C , LRG_319:g.38636A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.978A>C	ENSP00000490268.2:p.Pro326=
ENST00000585748.3:c.606A>C	ENSP00000477641.2:p.Pro202=
ENST00000585851.2:c.804A>C	ENSP00000467912.2:p.Pro268=
ENST00000326873.12:c.978A>C MANE Select	ENSP00000324856.6:p.Pro326=
ENST00000652231.1:c.978A>C	ENSP00000498804.1:p.Pro326=
ENST00000326873.11:c.978A>C	ENSP00000324856.6:p.Pro326=
ENST00000586243.5:c.978A>C	ENSP00000467240.2:p.Pro326=
ENST00000589152.5:n.1676A>C
ENST00000591133.2:n.949A>C
NM_000455.4:c.978A>C , LRG_319t1:c.978A>C	NP_000446.1:p.Pro326=
XM_005259617.1:c.978A>C	XP_005259674.1:p.Pro326=
XM_005259618.3:c.978A>C	XP_005259675.1:p.Pro326=
XM_011528209.1:c.756A>C	XP_011526511.1:p.Pro252=
XR_936204.1:n.1754A>C
XM_005259617.3:c.978A>C	XP_005259674.1:p.Pro326=
XM_011528209.2:c.756A>C	XP_011526511.1:p.Pro252=
XR_001753738.2:n.1784A>C
XR_001753739.1:n.1784A>C
XR_001753740.2:n.1754A>C
NM_000455.5:c.978A>C MANE Select	NP_000446.1:p.Pro326=