Canonical Allele Identifier: CA402953749

Gene: STK11

Linked Data

• ClinVar Variation Id: 527818
• ClinVar RCV Id: RCV000632812 ; RCV003302995
• dbSNP Id: rs1555740191
• MyVariant Identifiers: chr19:g.1226554T>C (hg19) ; chr19:g.1226555T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226555T>C , CM000681.2:g.1226555T>C	GRCh38
NC_000019.9:g.1226554T>C , CM000681.1:g.1226554T>C	GRCh37
NC_000019.8:g.1177554T>C	NCBI36
NG_007460.2:g.42149T>C , LRG_319:g.42149T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2811T>C	ENSP00000490268.2:n.*2811T>C
ENST00000585748.3:c.838T>C	ENSP00000477641.2:p.Ser280Pro
ENST00000585851.2:c.1036T>C	ENSP00000467912.2:p.Ser346Pro
ENST00000326873.12:c.1210T>C MANE Select	ENSP00000324856.6:p.Ser404Pro
ENST00000326873.11:c.1210T>C	ENSP00000324856.6:p.Ser404Pro
ENST00000585465.2:n.2943T>C
ENST00000586243.5:c.1210T>C	ENSP00000467240.2:p.Ser404Pro
ENST00000589152.5:n.1908T>C
NM_000455.4:c.1210T>C , LRG_319t1:c.1210T>C	NP_000446.1:p.Ser404Pro
XM_005259617.1:c.1205T>C	XP_005259674.1:p.Ile402Thr
XM_011528209.1:c.983T>C	XP_011526511.1:p.Ile328Thr
XM_005259617.3:c.1205T>C	XP_005259674.1:p.Ile402Thr
XM_011528209.2:c.983T>C	XP_011526511.1:p.Ile328Thr
XR_001753738.2:n.2016T>C
XR_001753740.2:n.1986T>C
NM_000455.5:c.1210T>C MANE Select	NP_000446.1:p.Ser404Pro