Canonical Allele Identifier: CA504708532

Gene: STK11

Linked Data

• ClinVar Variation Id: 928038
• ClinVar RCV Id: RCV001191688
• dbSNP Id: rs184271025
• gnomAD v4: 19-1226539-G-T
• MyVariant Identifiers: chr19:g.1226538G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226539G>T , CM000681.2:g.1226539G>T	GRCh38
NC_000019.9:g.1226538G>T , CM000681.1:g.1226538G>T	GRCh37
NC_000019.8:g.1177538G>T	NCBI36
NG_007460.2:g.42133G>T , LRG_319:g.42133G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.*2795G>T	ENSP00000490268.2:n.*2795G>T
ENST00000585748.3:c.822G>T	ENSP00000477641.2:p.Ala274=
ENST00000585851.2:c.1020G>T	ENSP00000467912.2:p.Ala340=
ENST00000326873.12:c.1194G>T MANE Select	ENSP00000324856.6:p.Ala398=
ENST00000326873.11:c.1194G>T	ENSP00000324856.6:p.Ala398=
ENST00000585465.2:n.2927G>T
ENST00000586243.5:c.1194G>T	ENSP00000467240.2:p.Ala398=
ENST00000589152.5:n.1892G>T
NM_000455.4:c.1194G>T , LRG_319t1:c.1194G>T	NP_000446.1:p.Ala398=
XM_005259617.1:c.1189G>T	XP_005259674.1:p.Ala397Ser
XM_011528209.1:c.967G>T	XP_011526511.1:p.Ala323Ser
XM_005259617.3:c.1189G>T	XP_005259674.1:p.Ala397Ser
XM_011528209.2:c.967G>T	XP_011526511.1:p.Ala323Ser
XR_001753738.2:n.2000G>T
XR_001753740.2:n.1970G>T
NM_000455.5:c.1194G>T MANE Select	NP_000446.1:p.Ala398=