Canonical Allele Identifier: CA10583785

Gene: STK11

Linked Data

• ClinVar Variation Id: 237802
• ClinVar RCV Id: RCV000227440 ; RCV001179584 ; RCV001420890
• dbSNP Id: rs878853989
• gnomAD v2: 19-1219419-GC-G
• gnomAD v3: 19-1219420-GC-G
• gnomAD v4: 19-1219420-GC-G
• MyVariant Identifiers: chr19:g.1219420del (hg19) ; chr19:g.1219421del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219421del , CM000681.2:g.1219421del	GRCh38
NC_000019.9:g.1219420del , CM000681.1:g.1219420del	GRCh37
NC_000019.8:g.1170420del	NCBI36
NG_007460.2:g.35015del , LRG_319:g.35015del

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.464+8del	ENSP00000490268.2:n.464+8del
ENST00000585748.3:c.92+8del	ENSP00000477641.2:n.92+8del
ENST00000585851.2:c.291-952del	ENSP00000467912.2:n.291-952del
ENST00000326873.12:c.464+8del MANE Select	ENSP00000324856.6:n.464+8del
ENST00000652231.1:c.464+8del	ENSP00000498804.1:n.464+8del
ENST00000326873.11:c.464+8del	ENSP00000324856.6:n.464+8del
ENST00000585851.1:c.291-952del	ENSP00000467912.1:n.291-952del
ENST00000586243.5:c.464+8del	ENSP00000467240.2:n.464+8del
ENST00000586358.5:n.287+8del
ENST00000589152.5:n.554+8del
NM_000455.4:c.464+8del , LRG_319t1:c.464+8del	NP_000446.1:n.464+8del
XM_005259617.1:c.464+8del	XP_005259674.1:n.464+8del
XM_005259618.3:c.464+8del	XP_005259675.1:n.464+8del
XM_011528209.1:c.242+8del	XP_011526511.1:n.242+8del
XR_936204.1:n.1089+8del
XM_005259617.3:c.464+8del	XP_005259674.1:n.464+8del
XM_011528209.2:c.242+8del	XP_011526511.1:n.242+8del
XR_001753738.2:n.1089+8del
XR_001753739.1:n.1089+8del
XR_001753740.2:n.1089+8del
NM_000455.5:c.464+8del MANE Select	NP_000446.1:n.464+8del