Canonical Allele Identifier: CA304016521

Gene: STK11

Linked Data

• dbSNP Id: rs897073090
• gnomAD v3: 19-1206690-G-T
• gnomAD v4: 19-1206690-G-T
• MyVariant Identifiers: chr19:g.1206689G>T (hg19) ; chr19:g.1206690G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206690G>T , CM000681.2:g.1206690G>T	GRCh38
NC_000019.9:g.1206689G>T , CM000681.1:g.1206689G>T	GRCh37
NC_000019.8:g.1157689G>T	NCBI36
NG_007460.2:g.22284G>T , LRG_319:g.22284G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.-224G>T	ENSP00000490268.2:n.-224G>T
ENST00000585748.3:c.-82-11727G>T	ENSP00000477641.2:n.-82-11727G>T
ENST00000326873.12:c.-224G>T MANE Select	ENSP00000324856.6:n.-224G>T
ENST00000652231.1:c.-224G>T	ENSP00000498804.1:n.-224G>T
ENST00000326873.11:c.-224G>T	ENSP00000324856.6:n.-224G>T
ENST00000585748.2:c.-82-11727G>T	ENSP00000477641.1:n.-82-11727G>T
ENST00000586243.5:c.-224G>T	ENSP00000467240.2:n.-224G>T
NM_000455.4:c.-224G>T , LRG_319t1:c.-224G>T	NP_000446.1:n.-224G>T
XM_005259617.1:c.-224G>T	XP_005259674.1:n.-224G>T
XM_005259618.3:c.-224G>T	XP_005259675.1:n.-224G>T
XM_011528209.1:c.-577G>T	XP_011526511.1:n.-577G>T
XR_936204.1:n.402G>T
XM_005259617.3:c.-224G>T	XP_005259674.1:n.-224G>T
XM_011528209.2:c.-577G>T	XP_011526511.1:n.-577G>T
XR_001753738.2:n.402G>T
XR_001753739.1:n.402G>T
XR_001753740.2:n.402G>T
NM_000455.5:c.-224G>T MANE Select	NP_000446.1:n.-224G>T