Canonical Allele Identifier: CA16620757

Gene: STK11

Linked Data

• ClinVar Variation Id: 419878
• ClinVar RCV Id: RCV000482588 ; RCV000565927 ; RCV000685196
• dbSNP Id: rs1064794167
• MyVariant Identifiers: chr19:g.1226471_1226473del (hg19) ; chr19:g.1226472_1226474del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226472_1226474del , CM000681.2:g.1226472_1226474del	GRCh38
NC_000019.9:g.1226471_1226473del , CM000681.1:g.1226471_1226473del	GRCh37
NC_000019.8:g.1177471_1177473del	NCBI36
NG_007460.2:g.42066_42068del , LRG_319:g.42066_42068del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2728_*2730del	ENSP00000490268.2:n.*2728_*2730del
ENST00000585748.3:c.755_757del	ENSP00000477641.2:p.Glu252del
ENST00000585851.2:c.953_955del	ENSP00000467912.2:p.Glu318del
ENST00000326873.12:c.1127_1129del MANE Select	ENSP00000324856.6:p.Glu376del
ENST00000326873.11:c.1127_1129del	ENSP00000324856.6:p.Glu376del
ENST00000585465.2:n.2860_2862del
ENST00000586243.5:c.1127_1129del	ENSP00000467240.2:p.Glu376del
ENST00000589152.5:n.1825_1827del
NM_000455.4:c.1127_1129del , LRG_319t1:c.1127_1129del	NP_000446.1:p.Glu376del
XM_005259617.1:c.1122_1124del	XP_005259674.1:p.Gly375del
XM_011528209.1:c.900_902del	XP_011526511.1:p.Gly301del
XM_005259617.3:c.1122_1124del	XP_005259674.1:p.Gly375del
XM_011528209.2:c.900_902del	XP_011526511.1:p.Gly301del
XR_001753738.2:n.1933_1935del
XR_001753740.2:n.1903_1905del
NM_000455.5:c.1127_1129del MANE Select	NP_000446.1:p.Glu376del