Canonical Allele Identifier: CA504707792

Gene: STK11

Linked Data

• MyVariant Identifiers: chr19:g.1223137T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1223138T>C , CM000681.2:g.1223138T>C	GRCh38
NC_000019.9:g.1223137T>C , CM000681.1:g.1223137T>C	GRCh37
NC_000019.8:g.1174137T>C	NCBI36
NG_007460.2:g.38732T>C , LRG_319:g.38732T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.1074T>C	ENSP00000490268.2:p.Asp358=
ENST00000585748.3:c.702T>C	ENSP00000477641.2:p.Asp234=
ENST00000585851.2:c.900T>C	ENSP00000467912.2:p.Asp300=
ENST00000326873.12:c.1074T>C MANE Select	ENSP00000324856.6:p.Asp358=
ENST00000652231.1:c.1074T>C	ENSP00000498804.1:p.Asp358=
ENST00000326873.11:c.1074T>C	ENSP00000324856.6:p.Asp358=
ENST00000586243.5:c.1074T>C	ENSP00000467240.2:p.Asp358=
ENST00000589152.5:n.1772T>C
NM_000455.4:c.1074T>C , LRG_319t1:c.1074T>C	NP_000446.1:p.Asp358=
XM_005259617.1:c.1074T>C	XP_005259674.1:p.Asp358=
XM_005259618.3:c.1074T>C	XP_005259675.1:p.Asp358=
XM_011528209.1:c.852T>C	XP_011526511.1:p.Asp284=
XR_936204.1:n.1850T>C
XM_005259617.3:c.1074T>C	XP_005259674.1:p.Asp358=
XM_011528209.2:c.852T>C	XP_011526511.1:p.Asp284=
XR_001753738.2:n.1880T>C
XR_001753739.1:n.1880T>C
XR_001753740.2:n.1850T>C
NM_000455.5:c.1074T>C MANE Select	NP_000446.1:p.Asp358=