Canonical Allele Identifier: CA783340637

Gene: STK11

Linked Data

• ClinVar Variation Id: 1697825
• ClinVar RCV Id: RCV002269109
• dbSNP Id: rs1446932431
• gnomAD v4: 19-1226429-GC-G
• MyVariant Identifiers: chr19:g.1226429del (hg19) ; chr19:g.1226430del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226431del , CM000681.2:g.1226431del	GRCh38
NC_000019.9:g.1226430del , CM000681.1:g.1226430del	GRCh37
NC_000019.8:g.1177430del	NCBI36
NG_007460.2:g.42025del , LRG_319:g.42025del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2687del	ENSP00000490268.2:n.*2687del
ENST00000585748.3:c.737-23del	ENSP00000477641.2:n.737-23del
ENST00000585851.2:c.935-23del	ENSP00000467912.2:n.935-23del
ENST00000326873.12:c.1109-23del MANE Select	ENSP00000324856.6:n.1109-23del
ENST00000326873.11:c.1109-23del	ENSP00000324856.6:n.1109-23del
ENST00000585465.2:n.2819del
ENST00000586243.5:c.1109-23del	ENSP00000467240.2:n.1109-23del
ENST00000589152.5:n.1807-23del
NM_000455.4:c.1109-23del , LRG_319t1:c.1109-23del	NP_000446.1:n.1109-23del
XM_005259617.1:c.1109-28del	XP_005259674.1:n.1109-28del
XM_011528209.1:c.887-28del	XP_011526511.1:n.887-28del
XM_005259617.3:c.1109-28del	XP_005259674.1:n.1109-28del
XM_011528209.2:c.887-28del	XP_011526511.1:n.887-28del
XR_001753738.2:n.1915-23del
XR_001753740.2:n.1885-23del
NM_000455.5:c.1109-23del MANE Select	NP_000446.1:n.1109-23del