Canonical Allele Identifier: CA402953853

Gene: STK11

Linked Data

• ClinVar Variation Id: 818646
• ClinVar RCV Id: RCV001010437
• dbSNP Id: rs1555740211
• MyVariant Identifiers: chr19:g.1226571G>C (hg19) ; chr19:g.1226572G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226572G>C , CM000681.2:g.1226572G>C	GRCh38
NC_000019.9:g.1226571G>C , CM000681.1:g.1226571G>C	GRCh37
NC_000019.8:g.1177571G>C	NCBI36
NG_007460.2:g.42166G>C , LRG_319:g.42166G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2828G>C	ENSP00000490268.2:n.*2828G>C
ENST00000585748.3:c.855G>C	ENSP00000477641.2:p.Arg285=
ENST00000585851.2:c.1053G>C	ENSP00000467912.2:p.Arg351=
ENST00000326873.12:c.1227G>C MANE Select	ENSP00000324856.6:p.Arg409=
ENST00000326873.11:c.1227G>C	ENSP00000324856.6:p.Arg409=
ENST00000585465.2:n.2960G>C
ENST00000586243.5:c.1226G>C	ENSP00000467240.2:p.Gly409Ala
ENST00000589152.5:n.1925G>C
NM_000455.4:c.1227G>C , LRG_319t1:c.1227G>C	NP_000446.1:p.Arg409=
XM_005259617.1:c.1222G>C	XP_005259674.1:p.Gly408Arg
XM_011528209.1:c.1000G>C	XP_011526511.1:p.Gly334Arg
XM_005259617.3:c.1222G>C	XP_005259674.1:p.Gly408Arg
XM_011528209.2:c.1000G>C	XP_011526511.1:p.Gly334Arg
XR_001753738.2:n.2033G>C
XR_001753740.2:n.2003G>C
NM_000455.5:c.1227G>C MANE Select	NP_000446.1:p.Arg409=