Canonical Allele Identifier: CA504708430

Gene: STK11

Linked Data

• ClinVar Variation Id: 762035
• ClinVar RCV Id: RCV001444035
• dbSNP Id: rs786201491
• MyVariant Identifiers: chr19:g.1226496G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226497G>C , CM000681.2:g.1226497G>C	GRCh38
NC_000019.9:g.1226496G>C , CM000681.1:g.1226496G>C	GRCh37
NC_000019.8:g.1177496G>C	NCBI36
NG_007460.2:g.42091G>C , LRG_319:g.42091G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2753G>C	ENSP00000490268.2:n.*2753G>C
ENST00000585748.3:c.780G>C	ENSP00000477641.2:p.Arg260=
ENST00000585851.2:c.978G>C	ENSP00000467912.2:p.Arg326=
ENST00000326873.12:c.1152G>C MANE Select	ENSP00000324856.6:p.Arg384=
ENST00000326873.11:c.1152G>C	ENSP00000324856.6:p.Arg384=
ENST00000585465.2:n.2885G>C
ENST00000586243.5:c.1152G>C	ENSP00000467240.2:p.Arg384=
ENST00000589152.5:n.1850G>C
NM_000455.4:c.1152G>C , LRG_319t1:c.1152G>C	NP_000446.1:p.Arg384=
XM_005259617.1:c.1147G>C	XP_005259674.1:p.Gly383Arg
XM_011528209.1:c.925G>C	XP_011526511.1:p.Gly309Arg
XM_005259617.3:c.1147G>C	XP_005259674.1:p.Gly383Arg
XM_011528209.2:c.925G>C	XP_011526511.1:p.Gly309Arg
XR_001753738.2:n.1958G>C
XR_001753740.2:n.1928G>C
NM_000455.5:c.1152G>C MANE Select	NP_000446.1:p.Arg384=