Canonical Allele Identifier: CA402953792

Gene: STK11

Linked Data

• dbSNP Id: rs748202003
• gnomAD v4: 19-1226562-C-A
• MyVariant Identifiers: chr19:g.1226561C>A (hg19) ; chr19:g.1226562C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226562C>A , CM000681.2:g.1226562C>A	GRCh38
NC_000019.9:g.1226561C>A , CM000681.1:g.1226561C>A	GRCh37
NC_000019.8:g.1177561C>A	NCBI36
NG_007460.2:g.42156C>A , LRG_319:g.42156C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2818C>A	ENSP00000490268.2:n.*2818C>A
ENST00000585748.3:c.845C>A	ENSP00000477641.2:p.Ala282Glu
ENST00000585851.2:c.1043C>A	ENSP00000467912.2:p.Ala348Glu
ENST00000326873.12:c.1217C>A MANE Select	ENSP00000324856.6:p.Ala406Glu
ENST00000326873.11:c.1217C>A	ENSP00000324856.6:p.Ala406Glu
ENST00000585465.2:n.2950C>A
ENST00000586243.5:c.1217C>A	ENSP00000467240.2:p.Ala406Glu
ENST00000589152.5:n.1915C>A
NM_000455.4:c.1217C>A , LRG_319t1:c.1217C>A	NP_000446.1:p.Ala406Glu
XM_005259617.1:c.1212C>A	XP_005259674.1:p.Gly404=
XM_011528209.1:c.990C>A	XP_011526511.1:p.Gly330=
XM_005259617.3:c.1212C>A	XP_005259674.1:p.Gly404=
XM_011528209.2:c.990C>A	XP_011526511.1:p.Gly330=
XR_001753738.2:n.2023C>A
XR_001753740.2:n.1993C>A
NM_000455.5:c.1217C>A MANE Select	NP_000446.1:p.Ala406Glu