Canonical Allele Identifier: CA402954253

Gene: STK11

Linked Data

• MyVariant Identifiers: chr19:g.1226633G>C (hg19) ; chr19:g.1226634G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226634G>C , CM000681.2:g.1226634G>C	GRCh38
NC_000019.9:g.1226633G>C , CM000681.1:g.1226633G>C	GRCh37
NC_000019.8:g.1177633G>C	NCBI36
NG_007460.2:g.42228G>C , LRG_319:g.42228G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.*2890G>C	ENSP00000490268.2:n.*2890G>C
ENST00000585748.3:c.917G>C	ENSP00000477641.2:p.Cys306Ser
ENST00000585851.2:c.1115G>C	ENSP00000467912.2:p.Cys372Ser
ENST00000326873.12:c.1289G>C MANE Select	ENSP00000324856.6:p.Cys430Ser
ENST00000326873.11:c.1289G>C	ENSP00000324856.6:p.Cys430Ser
ENST00000585465.2:n.3022G>C
ENST00000586243.5:c.1286G>C	ENSP00000467240.2:p.Cys429Ser
ENST00000589152.5:n.1987G>C
NM_000455.4:c.1289G>C , LRG_319t1:c.1289G>C	NP_000446.1:p.Cys430Ser
XM_005259617.1:c.1284G>C	XP_005259674.1:p.Leu428=
XM_011528209.1:c.1062G>C	XP_011526511.1:p.Leu354=
XM_005259617.3:c.1284G>C	XP_005259674.1:p.Leu428=
XM_011528209.2:c.1062G>C	XP_011526511.1:p.Leu354=
XR_001753738.2:n.2095G>C
XR_001753740.2:n.2065G>C
NM_000455.5:c.1289G>C MANE Select	NP_000446.1:p.Cys430Ser