Canonical Allele Identifier: CA402953460

Gene: STK11

Linked Data

• MyVariant Identifiers: chr19:g.1226508G>C (hg19) ; chr19:g.1226509G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226509G>C , CM000681.2:g.1226509G>C	GRCh38
NC_000019.9:g.1226508G>C , CM000681.1:g.1226508G>C	GRCh37
NC_000019.8:g.1177508G>C	NCBI36
NG_007460.2:g.42103G>C , LRG_319:g.42103G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2765G>C	ENSP00000490268.2:n.*2765G>C
ENST00000585748.3:c.792G>C	ENSP00000477641.2:p.Lys264Asn
ENST00000585851.2:c.990G>C	ENSP00000467912.2:p.Lys330Asn
ENST00000326873.12:c.1164G>C MANE Select	ENSP00000324856.6:p.Lys388Asn
ENST00000326873.11:c.1164G>C	ENSP00000324856.6:p.Lys388Asn
ENST00000585465.2:n.2897G>C
ENST00000586243.5:c.1164G>C	ENSP00000467240.2:p.Lys388Asn
ENST00000589152.5:n.1862G>C
NM_000455.4:c.1164G>C , LRG_319t1:c.1164G>C	NP_000446.1:p.Lys388Asn
XM_005259617.1:c.1159G>C	XP_005259674.1:p.Gly387Arg
XM_011528209.1:c.937G>C	XP_011526511.1:p.Gly313Arg
XM_005259617.3:c.1159G>C	XP_005259674.1:p.Gly387Arg
XM_011528209.2:c.937G>C	XP_011526511.1:p.Gly313Arg
XR_001753738.2:n.1970G>C
XR_001753740.2:n.1940G>C
NM_000455.5:c.1164G>C MANE Select	NP_000446.1:p.Lys388Asn