Canonical Allele Identifier: CA402953649

Gene: STK11

Linked Data

• gnomAD v4: 19-1226540-C-T
• MyVariant Identifiers: chr19:g.1226539C>T (hg19) ; chr19:g.1226540C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226540C>T , CM000681.2:g.1226540C>T	GRCh38
NC_000019.9:g.1226539C>T , CM000681.1:g.1226539C>T	GRCh37
NC_000019.8:g.1177539C>T	NCBI36
NG_007460.2:g.42134C>T , LRG_319:g.42134C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2796C>T	ENSP00000490268.2:n.*2796C>T
ENST00000585748.3:c.823C>T	ENSP00000477641.2:p.Gln275Ter
ENST00000585851.2:c.1021C>T	ENSP00000467912.2:p.Gln341Ter
ENST00000326873.12:c.1195C>T MANE Select	ENSP00000324856.6:p.Gln399Ter
ENST00000326873.11:c.1195C>T	ENSP00000324856.6:p.Gln399Ter
ENST00000585465.2:n.2928C>T
ENST00000586243.5:c.1195C>T	ENSP00000467240.2:p.Gln399Ter
ENST00000589152.5:n.1893C>T
NM_000455.4:c.1195C>T , LRG_319t1:c.1195C>T	NP_000446.1:p.Gln399Ter
XM_005259617.1:c.1190C>T	XP_005259674.1:p.Ala397Val
XM_011528209.1:c.968C>T	XP_011526511.1:p.Ala323Val
XM_005259617.3:c.1190C>T	XP_005259674.1:p.Ala397Val
XM_011528209.2:c.968C>T	XP_011526511.1:p.Ala323Val
XR_001753738.2:n.2001C>T
XR_001753740.2:n.1971C>T
NM_000455.5:c.1195C>T MANE Select	NP_000446.1:p.Gln399Ter