Canonical Allele Identifier: CA402953658

Gene: STK11

Linked Data

• dbSNP Id: rs2145436171
• MyVariant Identifiers: chr19:g.1226540A>T (hg19) ; chr19:g.1226541A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226541A>T , CM000681.2:g.1226541A>T	GRCh38
NC_000019.9:g.1226540A>T , CM000681.1:g.1226540A>T	GRCh37
NC_000019.8:g.1177540A>T	NCBI36
NG_007460.2:g.42135A>T , LRG_319:g.42135A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2797A>T	ENSP00000490268.2:n.*2797A>T
ENST00000585748.3:c.824A>T	ENSP00000477641.2:p.Gln275Leu
ENST00000585851.2:c.1022A>T	ENSP00000467912.2:p.Gln341Leu
ENST00000326873.12:c.1196A>T MANE Select	ENSP00000324856.6:p.Gln399Leu
ENST00000326873.11:c.1196A>T	ENSP00000324856.6:p.Gln399Leu
ENST00000585465.2:n.2929A>T
ENST00000586243.5:c.1196A>T	ENSP00000467240.2:p.Gln399Leu
ENST00000589152.5:n.1894A>T
NM_000455.4:c.1196A>T , LRG_319t1:c.1196A>T	NP_000446.1:p.Gln399Leu
XM_005259617.1:c.1191A>T	XP_005259674.1:p.Ala397=
XM_011528209.1:c.969A>T	XP_011526511.1:p.Ala323=
XM_005259617.3:c.1191A>T	XP_005259674.1:p.Ala397=
XM_011528209.2:c.969A>T	XP_011526511.1:p.Ala323=
XR_001753738.2:n.2002A>T
XR_001753740.2:n.1972A>T
NM_000455.5:c.1196A>T MANE Select	NP_000446.1:p.Gln399Leu