Canonical Allele Identifier: CA402954093

Gene: STK11

Linked Data

• dbSNP Id: rs1253803683
• MyVariant Identifiers: chr19:g.1226606G>C (hg19) ; chr19:g.1226607G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226607G>C , CM000681.2:g.1226607G>C	GRCh38
NC_000019.9:g.1226606G>C , CM000681.1:g.1226606G>C	GRCh37
NC_000019.8:g.1177606G>C	NCBI36
NG_007460.2:g.42201G>C , LRG_319:g.42201G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2863G>C	ENSP00000490268.2:n.*2863G>C
ENST00000585748.3:c.890G>C	ENSP00000477641.2:p.Ser297Thr
ENST00000585851.2:c.1088G>C	ENSP00000467912.2:p.Ser363Thr
ENST00000326873.12:c.1262G>C MANE Select	ENSP00000324856.6:p.Ser421Thr
ENST00000326873.11:c.1262G>C	ENSP00000324856.6:p.Ser421Thr
ENST00000585465.2:n.2995G>C
ENST00000586243.5:c.1259G>C	ENSP00000467240.2:p.Ser420Thr
ENST00000589152.5:n.1960G>C
NM_000455.4:c.1262G>C , LRG_319t1:c.1262G>C	NP_000446.1:p.Ser421Thr
XM_005259617.1:c.1257G>C	XP_005259674.1:p.Gln419His
XM_011528209.1:c.1035G>C	XP_011526511.1:p.Gln345His
XM_005259617.3:c.1257G>C	XP_005259674.1:p.Gln419His
XM_011528209.2:c.1035G>C	XP_011526511.1:p.Gln345His
XR_001753738.2:n.2068G>C
XR_001753740.2:n.2038G>C
NM_000455.5:c.1262G>C MANE Select	NP_000446.1:p.Ser421Thr