Canonical Allele Identifier: CA402953910

Gene: STK11

Linked Data

• ClinVar Variation Id: 851866
• ClinVar RCV Id: RCV001056363
• dbSNP Id: rs1158714606
• MyVariant Identifiers: chr19:g.1226580C>G (hg19) ; chr19:g.1226581C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226581C>G , CM000681.2:g.1226581C>G	GRCh38
NC_000019.9:g.1226580C>G , CM000681.1:g.1226580C>G	GRCh37
NC_000019.8:g.1177580C>G	NCBI36
NG_007460.2:g.42175C>G , LRG_319:g.42175C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2837C>G	ENSP00000490268.2:n.*2837C>G
ENST00000585748.3:c.864C>G	ENSP00000477641.2:p.Asn288Lys
ENST00000585851.2:c.1062C>G	ENSP00000467912.2:p.Asn354Lys
ENST00000326873.12:c.1236C>G MANE Select	ENSP00000324856.6:p.Asn412Lys
ENST00000326873.11:c.1236C>G	ENSP00000324856.6:p.Asn412Lys
ENST00000585465.2:n.2969C>G
ENST00000586243.5:c.1235C>G	ENSP00000467240.2:p.Thr412Ser
ENST00000589152.5:n.1934C>G
NM_000455.4:c.1236C>G , LRG_319t1:c.1236C>G	NP_000446.1:p.Asn412Lys
XM_005259617.1:c.1231C>G	XP_005259674.1:p.Pro411Ala
XM_011528209.1:c.1009C>G	XP_011526511.1:p.Pro337Ala
XM_005259617.3:c.1231C>G	XP_005259674.1:p.Pro411Ala
XM_011528209.2:c.1009C>G	XP_011526511.1:p.Pro337Ala
XR_001753738.2:n.2042C>G
XR_001753740.2:n.2012C>G
NM_000455.5:c.1236C>G MANE Select	NP_000446.1:p.Asn412Lys