Canonical Allele Identifier: CA658656740

Gene: STK11

Linked Data

• ClinVar Variation Id: 485010
• ClinVar RCV Id: RCV000563941
• dbSNP Id: rs1555737444
• MyVariant Identifiers: chr19:g.1218482del (hg19) ; chr19:g.1218483del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218483del , CM000681.2:g.1218483del	GRCh38
NC_000019.9:g.1218482del , CM000681.1:g.1218482del	GRCh37
NC_000019.8:g.1169482del	NCBI36
NG_007460.2:g.34077del , LRG_319:g.34077del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.357del	ENSP00000490268.2:p.Asn119LysfsTer10
ENST00000585748.3:c.-16del	ENSP00000477641.2:n.-16del
ENST00000585851.2:c.291-1890del	ENSP00000467912.2:n.291-1890del
ENST00000326873.12:c.357del MANE Select	ENSP00000324856.6:p.Asn119LysfsTer10
ENST00000652231.1:c.357del	ENSP00000498804.1:p.Asn119LysfsTer10
ENST00000326873.11:c.357del	ENSP00000324856.6:p.Asn119LysfsTer10
ENST00000585748.2:c.-16del	ENSP00000477641.1:n.-16del
ENST00000585851.1:c.291-1890del	ENSP00000467912.1:n.291-1890del
ENST00000586243.5:c.357del	ENSP00000467240.2:p.Asn119LysfsTer10
ENST00000586358.5:n.180del
ENST00000589152.5:n.447del
ENST00000593219.5:c.*182del	ENSP00000466610.1:n.*182del
NM_000455.4:c.357del , LRG_319t1:c.357del	NP_000446.1:p.Asn119LysfsTer10
XM_005259617.1:c.357del	XP_005259674.1:p.Asn119LysfsTer10
XM_005259618.3:c.357del	XP_005259675.1:p.Asn119LysfsTer10
XM_011528209.1:c.135del	XP_011526511.1:p.Asn45LysfsTer10
XR_936204.1:n.982del
XM_005259617.3:c.357del	XP_005259674.1:p.Asn119LysfsTer10
XM_011528209.2:c.135del	XP_011526511.1:p.Asn45LysfsTer10
XR_001753738.2:n.982del
XR_001753739.1:n.982del
XR_001753740.2:n.982del
NM_000455.5:c.357del MANE Select	NP_000446.1:p.Asn119LysfsTer10