Canonical Allele Identifier: CA915951607

Gene: STK11

Linked Data

• ClinVar Variation Id: 658263
• ClinVar RCV Id: RCV000815055
• dbSNP Id: rs1599914747

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206931_1206932delinsAA , CM000681.2:g.1206931_1206932delinsAA	GRCh38
NC_000019.9:g.1206930_1206931delinsAA , CM000681.1:g.1206930_1206931delinsAA	GRCh37
NC_000019.8:g.1157930_1157931delinsAA	NCBI36
NG_007460.2:g.22525_22526delinsAA , LRG_319:g.22525_22526delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.18_19delinsAA	ENSP00000490268.2:p.Gln7Lys
ENST00000585748.3:c.-82-11486_-82-11485delinsAA	ENSP00000477641.2:n.-82-11486_-82-11485delinsAA
ENST00000585851.2:c.18_19delinsAA	ENSP00000467912.2:p.Gln7Lys
ENST00000326873.12:c.18_19delinsAA MANE Select	ENSP00000324856.6:p.Gln7Lys
ENST00000652231.1:c.18_19delinsAA	ENSP00000498804.1:p.Gln7Lys
ENST00000326873.11:c.18_19delinsAA	ENSP00000324856.6:p.Gln7Lys
ENST00000585748.2:c.-82-11486_-82-11485delinsAA	ENSP00000477641.1:n.-82-11486_-82-11485delinsAA
ENST00000585851.1:c.18_19delinsAA	ENSP00000467912.1:p.Gln7Lys
ENST00000586243.5:c.18_19delinsAA	ENSP00000467240.2:p.Gln7Lys
ENST00000589152.5:n.108_109delinsAA
ENST00000593219.5:c.18_19delinsAA	ENSP00000466610.1:p.Gln7Lys
NM_000455.4:c.18_19delinsAA , LRG_319t1:c.18_19delinsAA	NP_000446.1:p.Gln7Lys
XM_005259617.1:c.18_19delinsAA	XP_005259674.1:p.Gln7Lys
XM_005259618.3:c.18_19delinsAA	XP_005259675.1:p.Gln7Lys
XM_011528209.1:c.-336_-335delinsAA	XP_011526511.1:n.-336_-335delinsAA
XR_936204.1:n.643_644delinsAA
XM_005259617.3:c.18_19delinsAA	XP_005259674.1:p.Gln7Lys
XM_011528209.2:c.-336_-335delinsAA	XP_011526511.1:n.-336_-335delinsAA
XR_001753738.2:n.643_644delinsAA
XR_001753739.1:n.643_644delinsAA
XR_001753740.2:n.643_644delinsAA
NM_000455.5:c.18_19delinsAA MANE Select	NP_000446.1:p.Gln7Lys