Canonical Allele Identifier: CA402954054

Gene: STK11

Linked Data

• dbSNP Id: rs375328708
• gnomAD v4: 19-1226602-C-A
• MyVariant Identifiers: chr19:g.1226601C>A (hg19) ; chr19:g.1226602C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226602C>A , CM000681.2:g.1226602C>A	GRCh38
NC_000019.9:g.1226601C>A , CM000681.1:g.1226601C>A	GRCh37
NC_000019.8:g.1177601C>A	NCBI36
NG_007460.2:g.42196C>A , LRG_319:g.42196C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2858C>A	ENSP00000490268.2:n.*2858C>A
ENST00000585748.3:c.885C>A	ENSP00000477641.2:p.Ser295=
ENST00000585851.2:c.1083C>A	ENSP00000467912.2:p.Ser361=
ENST00000326873.12:c.1257C>A MANE Select	ENSP00000324856.6:p.Ser419=
ENST00000326873.11:c.1257C>A	ENSP00000324856.6:p.Ser419=
ENST00000585465.2:n.2990C>A
ENST00000586243.5:c.1255-1C>A	ENSP00000467240.2:n.1255-1C>A
ENST00000589152.5:n.1955C>A
NM_000455.4:c.1257C>A , LRG_319t1:c.1257C>A	NP_000446.1:p.Ser419=
XM_005259617.1:c.1252C>A	XP_005259674.1:p.Arg418Ser
XM_011528209.1:c.1030C>A	XP_011526511.1:p.Arg344Ser
XM_005259617.3:c.1252C>A	XP_005259674.1:p.Arg418Ser
XM_011528209.2:c.1030C>A	XP_011526511.1:p.Arg344Ser
XR_001753738.2:n.2063C>A
XR_001753740.2:n.2033C>A
NM_000455.5:c.1257C>A MANE Select	NP_000446.1:p.Ser419=