Canonical Allele Identifier: CA402953384

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226496G>C , CM000681.2:g.1226496G>C	GRCh38
NC_000019.9:g.1226495G>C , CM000681.1:g.1226495G>C	GRCh37
NC_000019.8:g.1177495G>C	NCBI36
NG_007460.2:g.42090G>C , LRG_319:g.42090G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.5:c.1151G>C MANE Select	NP_000446.1:p.Arg384Pro
ENST00000326873.12:c.1151G>C MANE Select	ENSP00000324856.6:p.Arg384Pro
NM_000455.4:c.1151G>C , LRG_319t1:c.1151G>C	NP_000446.1:p.Arg384Pro
ENST00000326873.11:c.1151G>C	ENSP00000324856.6:p.Arg384Pro
ENST00000585465.2:n.2884G>C
ENST00000585465.3:c.*2752G>C	ENSP00000490268.2:n.*2752G>C
ENST00000585748.3:c.779G>C	ENSP00000477641.2:p.Arg260Pro
ENST00000585851.2:c.977G>C	ENSP00000467912.2:p.Arg326Pro
ENST00000586243.5:c.1151G>C	ENSP00000467240.2:p.Arg384Pro
ENST00000589152.5:n.1849G>C
XM_005259617.1:c.1146G>C	XP_005259674.1:p.Pro382=
XM_005259617.3:c.1146G>C	XP_005259674.1:p.Pro382=
XM_011528209.1:c.924G>C	XP_011526511.1:p.Pro308=
XM_011528209.2:c.924G>C	XP_011526511.1:p.Pro308=
XR_001753738.2:n.1957G>C
XR_001753740.2:n.1927G>C