Canonical Allele Identifier: CA402953387

Gene: STK11

Linked Data

• ClinVar Variation Id: 646005
• ClinVar RCV Id: RCV000800204
• dbSNP Id: rs371102112
• MyVariant Identifiers: chr19:g.1226495G>T (hg19) ; chr19:g.1226496G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226496G>T , CM000681.2:g.1226496G>T	GRCh38
NC_000019.9:g.1226495G>T , CM000681.1:g.1226495G>T	GRCh37
NC_000019.8:g.1177495G>T	NCBI36
NG_007460.2:g.42090G>T , LRG_319:g.42090G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2752G>T	ENSP00000490268.2:n.*2752G>T
ENST00000585748.3:c.779G>T	ENSP00000477641.2:p.Arg260Leu
ENST00000585851.2:c.977G>T	ENSP00000467912.2:p.Arg326Leu
ENST00000326873.12:c.1151G>T MANE Select	ENSP00000324856.6:p.Arg384Leu
ENST00000326873.11:c.1151G>T	ENSP00000324856.6:p.Arg384Leu
ENST00000585465.2:n.2884G>T
ENST00000586243.5:c.1151G>T	ENSP00000467240.2:p.Arg384Leu
ENST00000589152.5:n.1849G>T
NM_000455.4:c.1151G>T , LRG_319t1:c.1151G>T	NP_000446.1:p.Arg384Leu
XM_005259617.1:c.1146G>T	XP_005259674.1:p.Pro382=
XM_011528209.1:c.924G>T	XP_011526511.1:p.Pro308=
XM_005259617.3:c.1146G>T	XP_005259674.1:p.Pro382=
XM_011528209.2:c.924G>T	XP_011526511.1:p.Pro308=
XR_001753738.2:n.1957G>T
XR_001753740.2:n.1927G>T
NM_000455.5:c.1151G>T MANE Select	NP_000446.1:p.Arg384Leu