Canonical Allele Identifier: CA402953600

Gene: STK11

Linked Data

• MyVariant Identifiers: chr19:g.1226531A>C (hg19) ; chr19:g.1226532A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226532A>C , CM000681.2:g.1226532A>C	GRCh38
NC_000019.9:g.1226531A>C , CM000681.1:g.1226531A>C	GRCh37
NC_000019.8:g.1177531A>C	NCBI36
NG_007460.2:g.42126A>C , LRG_319:g.42126A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.*2788A>C	ENSP00000490268.2:n.*2788A>C
ENST00000585748.3:c.815A>C	ENSP00000477641.2:p.Glu272Ala
ENST00000585851.2:c.1013A>C	ENSP00000467912.2:p.Glu338Ala
ENST00000326873.12:c.1187A>C MANE Select	ENSP00000324856.6:p.Glu396Ala
ENST00000326873.11:c.1187A>C	ENSP00000324856.6:p.Glu396Ala
ENST00000585465.2:n.2920A>C
ENST00000586243.5:c.1187A>C	ENSP00000467240.2:p.Glu396Ala
ENST00000589152.5:n.1885A>C
NM_000455.4:c.1187A>C , LRG_319t1:c.1187A>C	NP_000446.1:p.Glu396Ala
XM_005259617.1:c.1182A>C	XP_005259674.1:p.Arg394Ser
XM_011528209.1:c.960A>C	XP_011526511.1:p.Arg320Ser
XM_005259617.3:c.1182A>C	XP_005259674.1:p.Arg394Ser
XM_011528209.2:c.960A>C	XP_011526511.1:p.Arg320Ser
XR_001753738.2:n.1993A>C
XR_001753740.2:n.1963A>C
NM_000455.5:c.1187A>C MANE Select	NP_000446.1:p.Glu396Ala