Canonical Allele Identifier: CA402953952

Gene: STK11

Linked Data

• ClinVar Variation Id: 1758613
• ClinVar RCV Id: RCV002380409 ; RCV003617984
• MyVariant Identifiers: chr19:g.1226586C>T (hg19) ; chr19:g.1226587C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226587C>T , CM000681.2:g.1226587C>T	GRCh38
NC_000019.9:g.1226586C>T , CM000681.1:g.1226586C>T	GRCh37
NC_000019.8:g.1177586C>T	NCBI36
NG_007460.2:g.42181C>T , LRG_319:g.42181C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2843C>T	ENSP00000490268.2:n.*2843C>T
ENST00000585748.3:c.870C>T	ENSP00000477641.2:p.Ala290=
ENST00000585851.2:c.1068C>T	ENSP00000467912.2:p.Ala356=
ENST00000326873.12:c.1242C>T MANE Select	ENSP00000324856.6:p.Ala414=
ENST00000326873.11:c.1242C>T	ENSP00000324856.6:p.Ala414=
ENST00000585465.2:n.2975C>T
ENST00000586243.5:c.1241C>T	ENSP00000467240.2:p.Pro414Leu
ENST00000589152.5:n.1940C>T
NM_000455.4:c.1242C>T , LRG_319t1:c.1242C>T	NP_000446.1:p.Ala414=
XM_005259617.1:c.1237C>T	XP_005259674.1:p.Pro413Ser
XM_011528209.1:c.1015C>T	XP_011526511.1:p.Pro339Ser
XM_005259617.3:c.1237C>T	XP_005259674.1:p.Pro413Ser
XM_011528209.2:c.1015C>T	XP_011526511.1:p.Pro339Ser
XR_001753738.2:n.2048C>T
XR_001753740.2:n.2018C>T
NM_000455.5:c.1242C>T MANE Select	NP_000446.1:p.Ala414=