Canonical Allele Identifier: CA402953401

Gene: STK11

Linked Data

• dbSNP Id: rs2080822137
• MyVariant Identifiers: chr19:g.1226498G>C (hg19) ; chr19:g.1226499G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226499G>C , CM000681.2:g.1226499G>C	GRCh38
NC_000019.9:g.1226498G>C , CM000681.1:g.1226498G>C	GRCh37
NC_000019.8:g.1177498G>C	NCBI36
NG_007460.2:g.42093G>C , LRG_319:g.42093G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2755G>C	ENSP00000490268.2:n.*2755G>C
ENST00000585748.3:c.782G>C	ENSP00000477641.2:p.Gly261Ala
ENST00000585851.2:c.980G>C	ENSP00000467912.2:p.Gly327Ala
ENST00000326873.12:c.1154G>C MANE Select	ENSP00000324856.6:p.Gly385Ala
ENST00000326873.11:c.1154G>C	ENSP00000324856.6:p.Gly385Ala
ENST00000585465.2:n.2887G>C
ENST00000586243.5:c.1154G>C	ENSP00000467240.2:p.Gly385Ala
ENST00000589152.5:n.1852G>C
NM_000455.4:c.1154G>C , LRG_319t1:c.1154G>C	NP_000446.1:p.Gly385Ala
XM_005259617.1:c.1149G>C	XP_005259674.1:p.Gly383=
XM_011528209.1:c.927G>C	XP_011526511.1:p.Gly309=
XM_005259617.3:c.1149G>C	XP_005259674.1:p.Gly383=
XM_011528209.2:c.927G>C	XP_011526511.1:p.Gly309=
XR_001753738.2:n.1960G>C
XR_001753740.2:n.1930G>C
NM_000455.5:c.1154G>C MANE Select	NP_000446.1:p.Gly385Ala