Canonical Allele Identifier: CA9039450

Gene: STK11

Linked Data

• dbSNP Id: rs752474669
• ExAC: 19:1218483 G / GGCCTAGGGACAGAGCAAGACTCTGTCTC
• MyVariant Identifiers: chr19:g.1218483_1218484insGCCTAGGGACAGAGCAAGACTCTGTCTC (hg19) ; chr19:g.1218484_1218485insGCCTAGGGACAGAGCAAGACTCTGTCTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218484_1218485insGCCTAGGGACAGAGCAAGACTCTGTCTC , CM000681.2:g.1218484_1218485insGCCTAGGGACAGAGCAAGACTCTGTCTC	GRCh38
NC_000019.9:g.1218483_1218484insGCCTAGGGACAGAGCAAGACTCTGTCTC , CM000681.1:g.1218483_1218484insGCCTAGGGACAGAGCAAGACTCTGTCTC	GRCh37
NC_000019.8:g.1169483_1169484insGCCTAGGGACAGAGCAAGACTCTGTCTC	NCBI36
NG_007460.2:g.34078_34079insGCCTAGGGACAGAGCAAGACTCTGTCTC , LRG_319:g.34078_34079insGCCTAGGGACAGAGCAAGACTCTGTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.358_359insGCCTAGGGACAGAGCAAGACTCTGTCTC	ENSP00000490268.2:p.Glu120GlyfsTer?
ENST00000585748.3:c.-15_-14insGCCTAGGGACAGAGCAAGACTCTGTCTC	ENSP00000477641.2:n.-15_-14insGCCTAGGGACAGAGCAAGACTCTGTCTC
ENST00000585851.2:c.291-1889_291-1888insGCCTAGGGACAGAGCAAGACTCTGTCTC	ENSP00000467912.2:n.291-1889_291-1888insGCCTAGGGACAGAGCAAGACT...
ENST00000326873.12:c.358_359insGCCTAGGGACAGAGCAAGACTCTGTCTC MANE Select	ENSP00000324856.6:p.Glu120GlyfsTer?
ENST00000652231.1:c.358_359insGCCTAGGGACAGAGCAAGACTCTGTCTC	ENSP00000498804.1:p.Glu120GlyfsTer?
ENST00000326873.11:c.358_359insGCCTAGGGACAGAGCAAGACTCTGTCTC	ENSP00000324856.6:p.Glu120GlyfsTer?
ENST00000585748.2:c.-15_-14insGCCTAGGGACAGAGCAAGACTCTGTCTC	ENSP00000477641.1:n.-15_-14insGCCTAGGGACAGAGCAAGACTCTGTCTC
ENST00000585851.1:c.291-1889_291-1888insGCCTAGGGACAGAGCAAGACTCTGTCTC	ENSP00000467912.1:n.291-1889_291-1888insGCCTAGGGACAGAGCAAGACT...
ENST00000586243.5:c.358_359insGCCTAGGGACAGAGCAAGACTCTGTCTC	ENSP00000467240.2:p.Glu120GlyfsTer?
ENST00000586358.5:n.181_182insGCCTAGGGACAGAGCAAGACTCTGTCTC
ENST00000589152.5:n.448_449insGCCTAGGGACAGAGCAAGACTCTGTCTC
ENST00000593219.5:c.*183_*184insGCCTAGGGACAGAGCAAGACTCTGTCTC	ENSP00000466610.1:n.*183_*184insGCCTAGGGACAGAGCAAGACTCTGTCTC
NM_000455.4:c.358_359insGCCTAGGGACAGAGCAAGACTCTGTCTC , LRG_319t1:c.358_359insGCCTAGGGACAGAGCAAGACTCTGTCTC	NP_000446.1:p.Glu120GlyfsTer?
XM_005259617.1:c.358_359insGCCTAGGGACAGAGCAAGACTCTGTCTC	XP_005259674.1:p.Glu120GlyfsTer?
XM_005259618.3:c.358_359insGCCTAGGGACAGAGCAAGACTCTGTCTC	XP_005259675.1:p.Glu120GlyfsTer?
XM_011528209.1:c.136_137insGCCTAGGGACAGAGCAAGACTCTGTCTC	XP_011526511.1:p.Glu46GlyfsTer?
XR_936204.1:n.983_984insGCCTAGGGACAGAGCAAGACTCTGTCTC
XM_005259617.3:c.358_359insGCCTAGGGACAGAGCAAGACTCTGTCTC	XP_005259674.1:p.Glu120GlyfsTer?
XM_011528209.2:c.136_137insGCCTAGGGACAGAGCAAGACTCTGTCTC	XP_011526511.1:p.Glu46GlyfsTer?
XR_001753738.2:n.983_984insGCCTAGGGACAGAGCAAGACTCTGTCTC
XR_001753739.1:n.983_984insGCCTAGGGACAGAGCAAGACTCTGTCTC
XR_001753740.2:n.983_984insGCCTAGGGACAGAGCAAGACTCTGTCTC
NM_000455.5:c.358_359insGCCTAGGGACAGAGCAAGACTCTGTCTC MANE Select	NP_000446.1:p.Glu120GlyfsTer?