Canonical Allele Identifier: CA402953862

Gene: STK11

Linked Data

• ClinVar Variation Id: 3231733
• ClinVar RCV Id: RCV004518448
• dbSNP Id: rs2080823389
• MyVariant Identifiers: chr19:g.1226572G>C (hg19) ; chr19:g.1226573G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226573G>C , CM000681.2:g.1226573G>C	GRCh38
NC_000019.9:g.1226572G>C , CM000681.1:g.1226572G>C	GRCh37
NC_000019.8:g.1177572G>C	NCBI36
NG_007460.2:g.42167G>C , LRG_319:g.42167G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2829G>C	ENSP00000490268.2:n.*2829G>C
ENST00000585748.3:c.856G>C	ENSP00000477641.2:p.Ala286Pro
ENST00000585851.2:c.1054G>C	ENSP00000467912.2:p.Ala352Pro
ENST00000326873.12:c.1228G>C MANE Select	ENSP00000324856.6:p.Ala410Pro
ENST00000326873.11:c.1228G>C	ENSP00000324856.6:p.Ala410Pro
ENST00000585465.2:n.2961G>C
ENST00000586243.5:c.1227G>C	ENSP00000467240.2:p.Gly409=
ENST00000589152.5:n.1926G>C
NM_000455.4:c.1228G>C , LRG_319t1:c.1228G>C	NP_000446.1:p.Ala410Pro
XM_005259617.1:c.1223G>C	XP_005259674.1:p.Gly408Ala
XM_011528209.1:c.1001G>C	XP_011526511.1:p.Gly334Ala
XM_005259617.3:c.1223G>C	XP_005259674.1:p.Gly408Ala
XM_011528209.2:c.1001G>C	XP_011526511.1:p.Gly334Ala
XR_001753738.2:n.2034G>C
XR_001753740.2:n.2004G>C
NM_000455.5:c.1228G>C MANE Select	NP_000446.1:p.Ala410Pro