Canonical Allele Identifier: CA631299710

Gene: STK11

Linked Data

• ClinVar Variation Id: 803512
• ClinVar RCV Id: RCV000990122
• dbSNP Id: rs1273032629
• gnomAD v2: 19-1206746-C-T
• gnomAD v3: 19-1206747-C-T
• gnomAD v4: 19-1206747-C-T
• MyVariant Identifiers: chr19:g.1206746C>T (hg19) ; chr19:g.1206747C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206747C>T , CM000681.2:g.1206747C>T	GRCh38
NC_000019.9:g.1206746C>T , CM000681.1:g.1206746C>T	GRCh37
NC_000019.8:g.1157746C>T	NCBI36
NG_007460.2:g.22341C>T , LRG_319:g.22341C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.-167C>T	ENSP00000490268.2:n.-167C>T
ENST00000585748.3:c.-82-11670C>T	ENSP00000477641.2:n.-82-11670C>T
ENST00000326873.12:c.-167C>T MANE Select	ENSP00000324856.6:n.-167C>T
ENST00000652231.1:c.-167C>T	ENSP00000498804.1:n.-167C>T
ENST00000326873.11:c.-167C>T	ENSP00000324856.6:n.-167C>T
ENST00000585748.2:c.-82-11670C>T	ENSP00000477641.1:n.-82-11670C>T
ENST00000586243.5:c.-167C>T	ENSP00000467240.2:n.-167C>T
NM_000455.4:c.-167C>T , LRG_319t1:c.-167C>T	NP_000446.1:n.-167C>T
XM_005259617.1:c.-167C>T	XP_005259674.1:n.-167C>T
XM_005259618.3:c.-167C>T	XP_005259675.1:n.-167C>T
XM_011528209.1:c.-520C>T	XP_011526511.1:n.-520C>T
XR_936204.1:n.459C>T
XM_005259617.3:c.-167C>T	XP_005259674.1:n.-167C>T
XM_011528209.2:c.-520C>T	XP_011526511.1:n.-520C>T
XR_001753738.2:n.459C>T
XR_001753739.1:n.459C>T
XR_001753740.2:n.459C>T
NM_000455.5:c.-167C>T MANE Select	NP_000446.1:n.-167C>T