Canonical Allele Identifier: CA022373

Gene: STK11

Linked Data

• ClinVar Variation Id: 184481
• ClinVar RCV Id: RCV000163744 ; RCV002053952
• dbSNP Id: rs786201491
• gnomAD v4: 19-1226497-G-T
• MyVariant Identifiers: chr19:g.1226496G>T (hg19) ; chr19:g.1226497G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226497G>T , CM000681.2:g.1226497G>T	GRCh38
NC_000019.9:g.1226496G>T , CM000681.1:g.1226496G>T	GRCh37
NC_000019.8:g.1177496G>T	NCBI36
NG_007460.2:g.42091G>T , LRG_319:g.42091G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2753G>T	ENSP00000490268.2:n.*2753G>T
ENST00000585748.3:c.780G>T	ENSP00000477641.2:p.Arg260=
ENST00000585851.2:c.978G>T	ENSP00000467912.2:p.Arg326=
ENST00000326873.12:c.1152G>T MANE Select	ENSP00000324856.6:p.Arg384=
ENST00000326873.11:c.1152G>T	ENSP00000324856.6:p.Arg384=
ENST00000585465.2:n.2885G>T
ENST00000586243.5:c.1152G>T	ENSP00000467240.2:p.Arg384=
ENST00000589152.5:n.1850G>T
NM_000455.4:c.1152G>T , LRG_319t1:c.1152G>T	NP_000446.1:p.Arg384=
XM_005259617.1:c.1147G>T	XP_005259674.1:p.Gly383Trp
XM_011528209.1:c.925G>T	XP_011526511.1:p.Gly309Trp
XM_005259617.3:c.1147G>T	XP_005259674.1:p.Gly383Trp
XM_011528209.2:c.925G>T	XP_011526511.1:p.Gly309Trp
XR_001753738.2:n.1958G>T
XR_001753740.2:n.1928G>T
NM_000455.5:c.1152G>T MANE Select	NP_000446.1:p.Arg384=