Canonical Allele Identifier: CA16608093

Gene: STK11

Linked Data

• ClinVar Variation Id: 388813
• ClinVar RCV Id: RCV000424168 ; RCV002522470
• dbSNP Id: rs568152768
• MyVariant Identifiers: chr19:g.1226440G>T (hg19) ; chr19:g.1226441G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226441G>T , CM000681.2:g.1226441G>T	GRCh38
NC_000019.9:g.1226440G>T , CM000681.1:g.1226440G>T	GRCh37
NC_000019.8:g.1177440G>T	NCBI36
NG_007460.2:g.42035G>T , LRG_319:g.42035G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2697G>T	ENSP00000490268.2:n.*2697G>T
ENST00000585748.3:c.737-13G>T	ENSP00000477641.2:n.737-13G>T
ENST00000585851.2:c.935-13G>T	ENSP00000467912.2:n.935-13G>T
ENST00000326873.12:c.1109-13G>T MANE Select	ENSP00000324856.6:n.1109-13G>T
ENST00000326873.11:c.1109-13G>T	ENSP00000324856.6:n.1109-13G>T
ENST00000585465.2:n.2829G>T
ENST00000586243.5:c.1109-13G>T	ENSP00000467240.2:n.1109-13G>T
ENST00000589152.5:n.1807-13G>T
NM_000455.4:c.1109-13G>T , LRG_319t1:c.1109-13G>T	NP_000446.1:n.1109-13G>T
XM_005259617.1:c.1109-18G>T	XP_005259674.1:n.1109-18G>T
XM_011528209.1:c.887-18G>T	XP_011526511.1:n.887-18G>T
XM_005259617.3:c.1109-18G>T	XP_005259674.1:n.1109-18G>T
XM_011528209.2:c.887-18G>T	XP_011526511.1:n.887-18G>T
XR_001753738.2:n.1915-13G>T
XR_001753740.2:n.1885-13G>T
NM_000455.5:c.1109-13G>T MANE Select	NP_000446.1:n.1109-13G>T