Canonical Allele Identifier: CA504707728

Gene: STK11

Linked Data

• ClinVar Variation Id: 922067
• ClinVar RCV Id: RCV001181915 ; RCV002068301
• dbSNP Id: rs376329042
• gnomAD v4: 19-1223009-G-T
• MyVariant Identifiers: chr19:g.1223008G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223009G>T , CM000681.2:g.1223009G>T	GRCh38
NC_000019.9:g.1223008G>T , CM000681.1:g.1223008G>T	GRCh37
NC_000019.8:g.1174008G>T	NCBI36
NG_007460.2:g.38603G>T , LRG_319:g.38603G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.945G>T	ENSP00000490268.2:p.Pro315=
ENST00000585748.3:c.573G>T	ENSP00000477641.2:p.Pro191=
ENST00000585851.2:c.771G>T	ENSP00000467912.2:p.Pro257=
ENST00000326873.12:c.945G>T MANE Select	ENSP00000324856.6:p.Pro315=
ENST00000652231.1:c.945G>T	ENSP00000498804.1:p.Pro315=
ENST00000326873.11:c.945G>T	ENSP00000324856.6:p.Pro315=
ENST00000586243.5:c.945G>T	ENSP00000467240.2:p.Pro315=
ENST00000589152.5:n.1643G>T
ENST00000591133.2:n.916G>T
NM_000455.4:c.945G>T , LRG_319t1:c.945G>T	NP_000446.1:p.Pro315=
XM_005259617.1:c.945G>T	XP_005259674.1:p.Pro315=
XM_005259618.3:c.945G>T	XP_005259675.1:p.Pro315=
XM_011528209.1:c.723G>T	XP_011526511.1:p.Pro241=
XR_936204.1:n.1721G>T
XM_005259617.3:c.945G>T	XP_005259674.1:p.Pro315=
XM_011528209.2:c.723G>T	XP_011526511.1:p.Pro241=
XR_001753738.2:n.1751G>T
XR_001753739.1:n.1751G>T
XR_001753740.2:n.1721G>T
NM_000455.5:c.945G>T MANE Select	NP_000446.1:p.Pro315=