Canonical Allele Identifier: CA304024006

Gene: STK11

Linked Data

• dbSNP Id: rs56814888
• gnomAD v2: 19-1218143-GA-G
• gnomAD v3: 19-1218144-GA-G
• gnomAD v4: 19-1218144-GA-G
• MyVariant Identifiers: chr19:g.1218144del (hg19) ; chr19:g.1218145del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218156del , CM000681.2:g.1218156del	GRCh38
NC_000019.9:g.1218155del , CM000681.1:g.1218155del	GRCh37
NC_000019.8:g.1169155del	NCBI36
NG_007460.2:g.33750del , LRG_319:g.33750del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.291-261del	ENSP00000490268.2:n.291-261del
ENST00000585748.3:c.-82-261del	ENSP00000477641.2:n.-82-261del
ENST00000585851.2:c.291-2217del	ENSP00000467912.2:n.291-2217del
ENST00000326873.12:c.291-261del MANE Select	ENSP00000324856.6:n.291-261del
ENST00000652231.1:c.291-261del	ENSP00000498804.1:n.291-261del
ENST00000326873.11:c.291-261del	ENSP00000324856.6:n.291-261del
ENST00000585748.2:c.-82-261del	ENSP00000477641.1:n.-82-261del
ENST00000585851.1:c.291-2217del	ENSP00000467912.1:n.291-2217del
ENST00000586243.5:c.291-261del	ENSP00000467240.2:n.291-261del
ENST00000586358.5:n.114-261del
ENST00000589152.5:n.381-261del
ENST00000593219.5:c.*116-261del	ENSP00000466610.1:n.*116-261del
NM_000455.4:c.291-261del , LRG_319t1:c.291-261del	NP_000446.1:n.291-261del
XM_005259617.1:c.291-261del	XP_005259674.1:n.291-261del
XM_005259618.3:c.291-261del	XP_005259675.1:n.291-261del
XM_011528209.1:c.69-261del	XP_011526511.1:n.69-261del
XR_936204.1:n.916-261del
XM_005259617.3:c.291-261del	XP_005259674.1:n.291-261del
XM_011528209.2:c.69-261del	XP_011526511.1:n.69-261del
XR_001753738.2:n.916-261del
XR_001753739.1:n.916-261del
XR_001753740.2:n.916-261del
NM_000455.5:c.291-261del MANE Select	NP_000446.1:n.291-261del