Canonical Allele Identifier: CA402954171

Gene: STK11

Linked Data

• dbSNP Id: rs2145436532
• MyVariant Identifiers: chr19:g.1226615T>C (hg19) ; chr19:g.1226616T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226616T>C , CM000681.2:g.1226616T>C	GRCh38
NC_000019.9:g.1226615T>C , CM000681.1:g.1226615T>C	GRCh37
NC_000019.8:g.1177615T>C	NCBI36
NG_007460.2:g.42210T>C , LRG_319:g.42210T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2872T>C	ENSP00000490268.2:n.*2872T>C
ENST00000585748.3:c.899T>C	ENSP00000477641.2:p.Ile300Thr
ENST00000585851.2:c.1097T>C	ENSP00000467912.2:p.Ile366Thr
ENST00000326873.12:c.1271T>C MANE Select	ENSP00000324856.6:p.Ile424Thr
ENST00000326873.11:c.1271T>C	ENSP00000324856.6:p.Ile424Thr
ENST00000585465.2:n.3004T>C
ENST00000586243.5:c.1268T>C	ENSP00000467240.2:p.Ile423Thr
ENST00000589152.5:n.1969T>C
NM_000455.4:c.1271T>C , LRG_319t1:c.1271T>C	NP_000446.1:p.Ile424Thr
XM_005259617.1:c.1266T>C	XP_005259674.1:p.Asp422=
XM_011528209.1:c.1044T>C	XP_011526511.1:p.Asp348=
XM_005259617.3:c.1266T>C	XP_005259674.1:p.Asp422=
XM_011528209.2:c.1044T>C	XP_011526511.1:p.Asp348=
XR_001753738.2:n.2077T>C
XR_001753740.2:n.2047T>C
NM_000455.5:c.1271T>C MANE Select	NP_000446.1:p.Ile424Thr