Canonical Allele Identifier: CA504708389

Gene: STK11

Linked Data

• MyVariant Identifiers: chr19:g.1226478T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226479T>C , CM000681.2:g.1226479T>C	GRCh38
NC_000019.9:g.1226478T>C , CM000681.1:g.1226478T>C	GRCh37
NC_000019.8:g.1177478T>C	NCBI36
NG_007460.2:g.42073T>C , LRG_319:g.42073T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2735T>C	ENSP00000490268.2:n.*2735T>C
ENST00000585748.3:c.762T>C	ENSP00000477641.2:p.Ser254=
ENST00000585851.2:c.960T>C	ENSP00000467912.2:p.Ser320=
ENST00000326873.12:c.1134T>C MANE Select	ENSP00000324856.6:p.Ser378=
ENST00000326873.11:c.1134T>C	ENSP00000324856.6:p.Ser378=
ENST00000585465.2:n.2867T>C
ENST00000586243.5:c.1134T>C	ENSP00000467240.2:p.Ser378=
ENST00000589152.5:n.1832T>C
NM_000455.4:c.1134T>C , LRG_319t1:c.1134T>C	NP_000446.1:p.Ser378=
XM_005259617.1:c.1129T>C	XP_005259674.1:p.Ser377Pro
XM_011528209.1:c.907T>C	XP_011526511.1:p.Ser303Pro
XM_005259617.3:c.1129T>C	XP_005259674.1:p.Ser377Pro
XM_011528209.2:c.907T>C	XP_011526511.1:p.Ser303Pro
XR_001753738.2:n.1940T>C
XR_001753740.2:n.1910T>C
NM_000455.5:c.1134T>C MANE Select	NP_000446.1:p.Ser378=