Canonical Allele Identifier: CA402954132

Gene: STK11

Linked Data

• MyVariant Identifiers: chr19:g.1226612A>C (hg19) ; chr19:g.1226613A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226613A>C , CM000681.2:g.1226613A>C	GRCh38
NC_000019.9:g.1226612A>C , CM000681.1:g.1226612A>C	GRCh37
NC_000019.8:g.1177612A>C	NCBI36
NG_007460.2:g.42207A>C , LRG_319:g.42207A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2869A>C	ENSP00000490268.2:n.*2869A>C
ENST00000585748.3:c.896A>C	ENSP00000477641.2:p.Lys299Thr
ENST00000585851.2:c.1094A>C	ENSP00000467912.2:p.Lys365Thr
ENST00000326873.12:c.1268A>C MANE Select	ENSP00000324856.6:p.Lys423Thr
ENST00000326873.11:c.1268A>C	ENSP00000324856.6:p.Lys423Thr
ENST00000585465.2:n.3001A>C
ENST00000586243.5:c.1265A>C	ENSP00000467240.2:p.Lys422Thr
ENST00000589152.5:n.1966A>C
NM_000455.4:c.1268A>C , LRG_319t1:c.1268A>C	NP_000446.1:p.Lys423Thr
XM_005259617.1:c.1263A>C	XP_005259674.1:p.Gln421His
XM_011528209.1:c.1041A>C	XP_011526511.1:p.Gln347His
XM_005259617.3:c.1263A>C	XP_005259674.1:p.Gln421His
XM_011528209.2:c.1041A>C	XP_011526511.1:p.Gln347His
XR_001753738.2:n.2074A>C
XR_001753740.2:n.2044A>C
NM_000455.5:c.1268A>C MANE Select	NP_000446.1:p.Lys423Thr